ENST00000265104.5:c.11468G>T
MANE Select
|
ENSP00000265104.4:p.Gly3823Val
|
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ENST00000681290.1:c.11423G>T
|
ENSP00000505288.1:p.Gly3808Val
|
|
ENST00000265104.4:c.11468G>T
|
ENSP00000265104.4:p.Gly3823Val
|
|
NM_001369.2:c.11468G>T
|
NP_001360.1:p.Gly3823Val
|
|
XM_005248262.2:c.11423G>T
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XP_005248319.1:p.Gly3808Val
|
|
XM_005248262.3:c.11576G>T
|
XP_005248319.2:p.Gly3859Val
|
|
XM_017009177.1:c.11576G>T
|
XP_016864666.1:p.Gly3859Val
|
|
XM_017009178.1:c.10481G>T
|
XP_016864667.1:p.Gly3494Val
|
|
XM_017009179.2:c.10481G>T
|
XP_016864668.1:p.Gly3494Val
|
|
XM_017009180.1:c.11576G>T
|
XP_016864669.1:p.Gly3859Val
|
|
XM_017009181.1:c.11576G>T
|
XP_016864670.1:p.Gly3859Val
|
|
XM_017009182.1:c.11332G>T
|
XP_016864671.1:p.Ala3778Ser
|
|
XM_017009185.1:c.6665G>T
|
XP_016864674.1:p.Gly2222Val
|
|
XM_017009186.1:c.6218G>T
|
XP_016864675.1:p.Gly2073Val
|
|
XM_017009188.1:c.5555G>T
|
XP_016864677.1:p.Gly1852Val
|
|
XM_024454388.1:c.10481G>T
|
XP_024310156.1:p.Gly3494Val
|
|
XM_024454389.1:c.10070G>T
|
XP_024310157.1:p.Gly3357Val
|
|
NM_001369.3:c.11468G>T
MANE Select
|
NP_001360.1:p.Gly3823Val
|
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