ENST00000683611.1:n.1093A>C
|
|
|
ENST00000265104.5:c.13760A>C
MANE Select
|
ENSP00000265104.4:p.Tyr4587Ser
|
|
ENST00000681290.1:c.13715A>C
|
ENSP00000505288.1:p.Tyr4572Ser
|
|
ENST00000265104.4:c.13760A>C
|
ENSP00000265104.4:p.Tyr4587Ser
|
|
NM_001369.2:c.13760A>C
|
NP_001360.1:p.Tyr4587Ser
|
|
XM_005248262.2:c.13715A>C
|
XP_005248319.1:p.Tyr4572Ser
|
|
XM_005248262.3:c.13868A>C
|
XP_005248319.2:p.Tyr4623Ser
|
|
XM_017009177.1:c.13448A>C
|
XP_016864666.1:p.Tyr4483Ser
|
|
XM_017009178.1:c.12773A>C
|
XP_016864667.1:p.Tyr4258Ser
|
|
XM_017009179.2:c.12773A>C
|
XP_016864668.1:p.Tyr4258Ser
|
|
XM_017009185.1:c.8957A>C
|
XP_016864674.1:p.Tyr2986Ser
|
|
XM_017009186.1:c.8510A>C
|
XP_016864675.1:p.Tyr2837Ser
|
|
XM_017009188.1:c.7847A>C
|
XP_016864677.1:p.Tyr2616Ser
|
|
XM_024454388.1:c.12773A>C
|
XP_024310156.1:p.Tyr4258Ser
|
|
XM_024454389.1:c.12362A>C
|
XP_024310157.1:p.Tyr4121Ser
|
|
NM_001369.3:c.13760A>C
MANE Select
|
NP_001360.1:p.Tyr4587Ser
|
|