ENST00000460843.6:c.2962G>T
MANE Select
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ENSP00000417980.1:p.Ala988Ser
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ENST00000636027.1:c.2848G>T
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ENSP00000489961.1:p.Ala950Ser
|
|
ENST00000637161.1:c.2869G>T
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ENSP00000490328.1:p.Ala957Ser
|
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ENST00000637261.1:c.3002G>T
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ENSP00000490815.1:n.3002G>T
|
|
ENST00000637891.1:c.856G>T
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ENSP00000490907.1:p.Ala286Ser
|
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ENST00000460843.5:c.2962G>T
|
ENSP00000417980.1:p.Ala988Ser
|
|
ENST00000462942.3:c.1819G>T
|
ENSP00000436107.1:p.Ala607Ser
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ENST00000486164.5:c.649G>T
|
|
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ENST00000488242.2:n.488G>T
|
|
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NM_024757.4:c.2962G>T
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NP_079033.4:p.Ala988Ser
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XM_005266105.3:c.2953G>T
|
XP_005266162.1:p.Ala985Ser
|
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XM_005266110.1:c.2869G>T
|
XP_005266167.1:p.Ala957Ser
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|
XM_006717288.2:c.2944G>T
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XP_006717351.1:p.Ala982Ser
|
|
XM_011519021.1:c.2971G>T
|
XP_011517323.1:p.Ala991Ser
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|
XM_011519022.1:c.2968G>T
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XP_011517324.1:p.Ala990Ser
|
|
XM_011519023.1:c.2950G>T
|
XP_011517325.1:p.Ala984Ser
|
|
XM_011519024.1:c.2893G>T
|
XP_011517326.1:p.Ala965Ser
|
|
XM_011519025.1:c.2869G>T
|
XP_011517327.1:p.Ala957Ser
|
|
XM_011519026.1:c.2827G>T
|
XP_011517328.1:p.Ala943Ser
|
|
XM_011519029.1:c.1393G>T
|
XP_011517331.1:p.Ala465Ser
|
|
XM_011519030.1:c.745G>T
|
XP_011517332.1:p.Ala249Ser
|
|
XM_011519031.1:c.532G>T
|
XP_011517333.1:p.Ala178Ser
|
|
XM_011519032.1:c.532G>T
|
XP_011517334.1:p.Ala178Ser
|
|
XM_011519033.1:c.2806G>T
|
XP_011517335.1:p.Ala936Ser
|
|
NM_001354263.1:c.2941G>T
|
NP_001341192.1:p.Ala981Ser
|
|
XM_005266105.5:c.2953G>T
|
XP_005266162.1:p.Ala985Ser
|
|
XM_011519021.3:c.2971G>T
|
XP_011517323.1:p.Ala991Ser
|
|
XM_011519022.3:c.2968G>T
|
XP_011517324.1:p.Ala990Ser
|
|
XM_011519023.3:c.2950G>T
|
XP_011517325.1:p.Ala984Ser
|
|
XM_011519029.3:c.1393G>T
|
XP_011517331.1:p.Ala465Ser
|
|
XM_011519030.3:c.745G>T
|
XP_011517332.1:p.Ala249Ser
|
|
XM_017015134.1:c.2947G>T
|
XP_016870623.1:p.Ala983Ser
|
|
XM_017015136.2:c.2863G>T
|
XP_016870625.1:p.Ala955Ser
|
|
XM_017015137.1:c.2848G>T
|
XP_016870626.1:p.Ala950Ser
|
|
XM_017015138.1:c.2848G>T
|
XP_016870627.1:p.Ala950Ser
|
|
XM_024447674.1:c.2791G>T
|
XP_024303442.1:p.Ala931Ser
|
|
XM_024447675.1:c.2725G>T
|
XP_024303443.1:p.Ala909Ser
|
|
XM_024447676.1:c.2086G>T
|
XP_024303444.1:p.Ala696Ser
|
|
XM_024447677.1:c.2086G>T
|
XP_024303445.1:p.Ala696Ser
|
|
XM_024447680.1:c.2704G>T
|
XP_024303448.1:p.Ala902Ser
|
|
NM_024757.5:c.2962G>T
MANE Select
|
NP_079033.4:p.Ala988Ser
|
|
NM_001354263.2:c.2941G>T
|
NP_001341192.1:p.Ala981Ser
|
|