ENST00000683611.1:n.1113G>C
|
|
|
ENST00000265104.5:c.13780G>C
MANE Select
|
ENSP00000265104.4:p.Asp4594His
|
|
ENST00000681290.1:c.13735G>C
|
ENSP00000505288.1:p.Asp4579His
|
|
ENST00000265104.4:c.13780G>C
|
ENSP00000265104.4:p.Asp4594His
|
|
NM_001369.2:c.13780G>C
|
NP_001360.1:p.Asp4594His
|
|
XM_005248262.2:c.13735G>C
|
XP_005248319.1:p.Asp4579His
|
|
XM_005248262.3:c.13888G>C
|
XP_005248319.2:p.Asp4630His
|
|
XM_017009177.1:c.13468G>C
|
XP_016864666.1:p.Asp4490His
|
|
XM_017009178.1:c.12793G>C
|
XP_016864667.1:p.Asp4265His
|
|
XM_017009179.2:c.12793G>C
|
XP_016864668.1:p.Asp4265His
|
|
XM_017009185.1:c.8977G>C
|
XP_016864674.1:p.Asp2993His
|
|
XM_017009186.1:c.8530G>C
|
XP_016864675.1:p.Asp2844His
|
|
XM_017009188.1:c.7867G>C
|
XP_016864677.1:p.Asp2623His
|
|
XM_024454388.1:c.12793G>C
|
XP_024310156.1:p.Asp4265His
|
|
XM_024454389.1:c.12382G>C
|
XP_024310157.1:p.Asp4128His
|
|
NM_001369.3:c.13780G>C
MANE Select
|
NP_001360.1:p.Asp4594His
|
|