ENST00000683611.1:n.1123A>G
|
|
|
ENST00000265104.5:c.13790A>G
MANE Select
|
ENSP00000265104.4:p.Tyr4597Cys
|
|
ENST00000681290.1:c.13745A>G
|
ENSP00000505288.1:p.Tyr4582Cys
|
|
ENST00000265104.4:c.13790A>G
|
ENSP00000265104.4:p.Tyr4597Cys
|
|
NM_001369.2:c.13790A>G
|
NP_001360.1:p.Tyr4597Cys
|
|
XM_005248262.2:c.13745A>G
|
XP_005248319.1:p.Tyr4582Cys
|
|
XM_005248262.3:c.13898A>G
|
XP_005248319.2:p.Tyr4633Cys
|
|
XM_017009177.1:c.13478A>G
|
XP_016864666.1:p.Tyr4493Cys
|
|
XM_017009178.1:c.12803A>G
|
XP_016864667.1:p.Tyr4268Cys
|
|
XM_017009179.2:c.12803A>G
|
XP_016864668.1:p.Tyr4268Cys
|
|
XM_017009185.1:c.8987A>G
|
XP_016864674.1:p.Tyr2996Cys
|
|
XM_017009186.1:c.8540A>G
|
XP_016864675.1:p.Tyr2847Cys
|
|
XM_017009188.1:c.7877A>G
|
XP_016864677.1:p.Tyr2626Cys
|
|
XM_024454388.1:c.12803A>G
|
XP_024310156.1:p.Tyr4268Cys
|
|
XM_024454389.1:c.12392A>G
|
XP_024310157.1:p.Tyr4131Cys
|
|
NM_001369.3:c.13790A>G
MANE Select
|
NP_001360.1:p.Tyr4597Cys
|
|