ENST00000683611.1:n.1105T>A
|
|
|
ENST00000265104.5:c.13772T>A
MANE Select
|
ENSP00000265104.4:p.Val4591Asp
|
|
ENST00000681290.1:c.13727T>A
|
ENSP00000505288.1:p.Val4576Asp
|
|
ENST00000265104.4:c.13772T>A
|
ENSP00000265104.4:p.Val4591Asp
|
|
NM_001369.2:c.13772T>A
|
NP_001360.1:p.Val4591Asp
|
|
XM_005248262.2:c.13727T>A
|
XP_005248319.1:p.Val4576Asp
|
|
XM_005248262.3:c.13880T>A
|
XP_005248319.2:p.Val4627Asp
|
|
XM_017009177.1:c.13460T>A
|
XP_016864666.1:p.Val4487Asp
|
|
XM_017009178.1:c.12785T>A
|
XP_016864667.1:p.Val4262Asp
|
|
XM_017009179.2:c.12785T>A
|
XP_016864668.1:p.Val4262Asp
|
|
XM_017009185.1:c.8969T>A
|
XP_016864674.1:p.Val2990Asp
|
|
XM_017009186.1:c.8522T>A
|
XP_016864675.1:p.Val2841Asp
|
|
XM_017009188.1:c.7859T>A
|
XP_016864677.1:p.Val2620Asp
|
|
XM_024454388.1:c.12785T>A
|
XP_024310156.1:p.Val4262Asp
|
|
XM_024454389.1:c.12374T>A
|
XP_024310157.1:p.Val4125Asp
|
|
NM_001369.3:c.13772T>A
MANE Select
|
NP_001360.1:p.Val4591Asp
|
|