ENST00000460843.6:c.2937G>C
MANE Select
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ENSP00000417980.1:p.Ala979=
|
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ENST00000636027.1:c.2823G>C
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ENSP00000489961.1:p.Ala941=
|
|
ENST00000637161.1:c.2844G>C
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ENSP00000490328.1:p.Ala948=
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ENST00000637261.1:c.2977G>C
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ENSP00000490815.1:n.2977G>C
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ENST00000637891.1:c.831G>C
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ENSP00000490907.1:p.Ala277=
|
|
ENST00000460843.5:c.2937G>C
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ENSP00000417980.1:p.Ala979=
|
|
ENST00000462942.3:c.1794G>C
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ENSP00000436107.1:p.Ala598=
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ENST00000486164.5:c.624G>C
|
|
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ENST00000488242.2:n.463G>C
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|
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NM_024757.4:c.2937G>C
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NP_079033.4:p.Ala979=
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|
XM_005266105.3:c.2928G>C
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XP_005266162.1:p.Ala976=
|
|
XM_005266110.1:c.2844G>C
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XP_005266167.1:p.Ala948=
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XM_006717288.2:c.2919G>C
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XP_006717351.1:p.Ala973=
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XM_011519021.1:c.2946G>C
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XP_011517323.1:p.Ala982=
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XM_011519022.1:c.2943G>C
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XP_011517324.1:p.Ala981=
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|
XM_011519023.1:c.2925G>C
|
XP_011517325.1:p.Ala975=
|
|
XM_011519024.1:c.2868G>C
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XP_011517326.1:p.Ala956=
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|
XM_011519025.1:c.2844G>C
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XP_011517327.1:p.Ala948=
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|
XM_011519026.1:c.2802G>C
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XP_011517328.1:p.Ala934=
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XM_011519029.1:c.1368G>C
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XP_011517331.1:p.Ala456=
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XM_011519030.1:c.720G>C
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XP_011517332.1:p.Ala240=
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XM_011519031.1:c.507G>C
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XP_011517333.1:p.Ala169=
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XM_011519032.1:c.507G>C
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XP_011517334.1:p.Ala169=
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|
XM_011519033.1:c.2781G>C
|
XP_011517335.1:p.Ala927=
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|
NM_001354263.1:c.2916G>C
|
NP_001341192.1:p.Ala972=
|
|
XM_005266105.5:c.2928G>C
|
XP_005266162.1:p.Ala976=
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|
XM_011519021.3:c.2946G>C
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XP_011517323.1:p.Ala982=
|
|
XM_011519022.3:c.2943G>C
|
XP_011517324.1:p.Ala981=
|
|
XM_011519023.3:c.2925G>C
|
XP_011517325.1:p.Ala975=
|
|
XM_011519029.3:c.1368G>C
|
XP_011517331.1:p.Ala456=
|
|
XM_011519030.3:c.720G>C
|
XP_011517332.1:p.Ala240=
|
|
XM_017015134.1:c.2922G>C
|
XP_016870623.1:p.Ala974=
|
|
XM_017015136.2:c.2838G>C
|
XP_016870625.1:p.Ala946=
|
|
XM_017015137.1:c.2823G>C
|
XP_016870626.1:p.Ala941=
|
|
XM_017015138.1:c.2823G>C
|
XP_016870627.1:p.Ala941=
|
|
XM_024447674.1:c.2766G>C
|
XP_024303442.1:p.Ala922=
|
|
XM_024447675.1:c.2700G>C
|
XP_024303443.1:p.Ala900=
|
|
XM_024447676.1:c.2061G>C
|
XP_024303444.1:p.Ala687=
|
|
XM_024447677.1:c.2061G>C
|
XP_024303445.1:p.Ala687=
|
|
XM_024447680.1:c.2679G>C
|
XP_024303448.1:p.Ala893=
|
|
NM_024757.5:c.2937G>C
MANE Select
|
NP_079033.4:p.Ala979=
|
|
NM_001354263.2:c.2916G>C
|
NP_001341192.1:p.Ala972=
|
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