ENST00000683611.1:n.1079C>G
|
|
|
ENST00000265104.5:c.13746C>G
MANE Select
|
ENSP00000265104.4:p.Tyr4582Ter
|
|
ENST00000681290.1:c.13701C>G
|
ENSP00000505288.1:p.Tyr4567Ter
|
|
ENST00000265104.4:c.13746C>G
|
ENSP00000265104.4:p.Tyr4582Ter
|
|
NM_001369.2:c.13746C>G
|
NP_001360.1:p.Tyr4582Ter
|
|
XM_005248262.2:c.13701C>G
|
XP_005248319.1:p.Tyr4567Ter
|
|
XM_005248262.3:c.13854C>G
|
XP_005248319.2:p.Tyr4618Ter
|
|
XM_017009177.1:c.13434C>G
|
XP_016864666.1:p.Tyr4478Ter
|
|
XM_017009178.1:c.12759C>G
|
XP_016864667.1:p.Tyr4253Ter
|
|
XM_017009179.2:c.12759C>G
|
XP_016864668.1:p.Tyr4253Ter
|
|
XM_017009185.1:c.8943C>G
|
XP_016864674.1:p.Tyr2981Ter
|
|
XM_017009186.1:c.8496C>G
|
XP_016864675.1:p.Tyr2832Ter
|
|
XM_017009188.1:c.7833C>G
|
XP_016864677.1:p.Tyr2611Ter
|
|
XM_024454388.1:c.12759C>G
|
XP_024310156.1:p.Tyr4253Ter
|
|
XM_024454389.1:c.12348C>G
|
XP_024310157.1:p.Tyr4116Ter
|
|
NM_001369.3:c.13746C>G
MANE Select
|
NP_001360.1:p.Tyr4582Ter
|
|