ENST00000683611.1:n.1077T>C
|
|
|
ENST00000265104.5:c.13744T>C
MANE Select
|
ENSP00000265104.4:p.Tyr4582His
|
|
ENST00000681290.1:c.13699T>C
|
ENSP00000505288.1:p.Tyr4567His
|
|
ENST00000265104.4:c.13744T>C
|
ENSP00000265104.4:p.Tyr4582His
|
|
NM_001369.2:c.13744T>C
|
NP_001360.1:p.Tyr4582His
|
|
XM_005248262.2:c.13699T>C
|
XP_005248319.1:p.Tyr4567His
|
|
XM_005248262.3:c.13852T>C
|
XP_005248319.2:p.Tyr4618His
|
|
XM_017009177.1:c.13432T>C
|
XP_016864666.1:p.Tyr4478His
|
|
XM_017009178.1:c.12757T>C
|
XP_016864667.1:p.Tyr4253His
|
|
XM_017009179.2:c.12757T>C
|
XP_016864668.1:p.Tyr4253His
|
|
XM_017009185.1:c.8941T>C
|
XP_016864674.1:p.Tyr2981His
|
|
XM_017009186.1:c.8494T>C
|
XP_016864675.1:p.Tyr2832His
|
|
XM_017009188.1:c.7831T>C
|
XP_016864677.1:p.Tyr2611His
|
|
XM_024454388.1:c.12757T>C
|
XP_024310156.1:p.Tyr4253His
|
|
XM_024454389.1:c.12346T>C
|
XP_024310157.1:p.Tyr4116His
|
|
NM_001369.3:c.13744T>C
MANE Select
|
NP_001360.1:p.Tyr4582His
|
|