ENST00000265104.5:c.12503T>A
MANE Select
|
ENSP00000265104.4:p.Val4168Asp
|
|
ENST00000681290.1:c.12458T>A
|
ENSP00000505288.1:p.Val4153Asp
|
|
ENST00000265104.4:c.12503T>A
|
ENSP00000265104.4:p.Val4168Asp
|
|
NM_001369.2:c.12503T>A
|
NP_001360.1:p.Val4168Asp
|
|
XM_005248262.2:c.12458T>A
|
XP_005248319.1:p.Val4153Asp
|
|
XM_005248262.3:c.12611T>A
|
XP_005248319.2:p.Val4204Asp
|
|
XM_017009177.1:c.12611T>A
|
XP_016864666.1:p.Val4204Asp
|
|
XM_017009178.1:c.11516T>A
|
XP_016864667.1:p.Val3839Asp
|
|
XM_017009179.2:c.11516T>A
|
XP_016864668.1:p.Val3839Asp
|
|
XM_017009180.1:c.12611T>A
|
XP_016864669.1:p.Val4204Asp
|
|
XM_017009185.1:c.7700T>A
|
XP_016864674.1:p.Val2567Asp
|
|
XM_017009186.1:c.7253T>A
|
XP_016864675.1:p.Val2418Asp
|
|
XM_017009188.1:c.6590T>A
|
XP_016864677.1:p.Val2197Asp
|
|
XM_024454388.1:c.11516T>A
|
XP_024310156.1:p.Val3839Asp
|
|
XM_024454389.1:c.11105T>A
|
XP_024310157.1:p.Val3702Asp
|
|
NM_001369.3:c.12503T>A
MANE Select
|
NP_001360.1:p.Val4168Asp
|
|