ENST00000265104.5:c.9569G>T
MANE Select
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ENSP00000265104.4:p.Gly3190Val
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ENST00000681290.1:c.9524G>T
|
ENSP00000505288.1:p.Gly3175Val
|
|
ENST00000265104.4:c.9569G>T
|
ENSP00000265104.4:p.Gly3190Val
|
|
ENST00000504001.3:n.281G>T
|
|
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NM_001369.2:c.9569G>T
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NP_001360.1:p.Gly3190Val
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XM_005248262.2:c.9524G>T
|
XP_005248319.1:p.Gly3175Val
|
|
XM_005248262.3:c.9677G>T
|
XP_005248319.2:p.Gly3226Val
|
|
XM_017009177.1:c.9677G>T
|
XP_016864666.1:p.Gly3226Val
|
|
XM_017009178.1:c.8582G>T
|
XP_016864667.1:p.Gly2861Val
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|
XM_017009179.2:c.8582G>T
|
XP_016864668.1:p.Gly2861Val
|
|
XM_017009180.1:c.9677G>T
|
XP_016864669.1:p.Gly3226Val
|
|
XM_017009181.1:c.9677G>T
|
XP_016864670.1:p.Gly3226Val
|
|
XM_017009182.1:c.9677G>T
|
XP_016864671.1:p.Gly3226Val
|
|
XM_017009183.1:c.9677G>T
|
XP_016864672.1:p.Gly3226Val
|
|
XM_017009185.1:c.4766G>T
|
XP_016864674.1:p.Gly1589Val
|
|
XM_017009186.1:c.4319G>T
|
XP_016864675.1:p.Gly1440Val
|
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XM_017009188.1:c.3656G>T
|
XP_016864677.1:p.Gly1219Val
|
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XM_024454388.1:c.8582G>T
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XP_024310156.1:p.Gly2861Val
|
|
XM_024454389.1:c.8171G>T
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XP_024310157.1:p.Gly2724Val
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NM_001369.3:c.9569G>T
MANE Select
|
NP_001360.1:p.Gly3190Val
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