ENST00000683611.1:n.1159C>A
|
|
|
ENST00000265104.5:c.13826C>A
MANE Select
|
ENSP00000265104.4:p.Pro4609His
|
|
ENST00000681290.1:c.13781C>A
|
ENSP00000505288.1:p.Pro4594His
|
|
ENST00000265104.4:c.13826C>A
|
ENSP00000265104.4:p.Pro4609His
|
|
NM_001369.2:c.13826C>A
|
NP_001360.1:p.Pro4609His
|
|
XM_005248262.2:c.13781C>A
|
XP_005248319.1:p.Pro4594His
|
|
XM_005248262.3:c.13934C>A
|
XP_005248319.2:p.Pro4645His
|
|
XM_017009177.1:c.13514C>A
|
XP_016864666.1:p.Pro4505His
|
|
XM_017009178.1:c.12839C>A
|
XP_016864667.1:p.Pro4280His
|
|
XM_017009179.2:c.12839C>A
|
XP_016864668.1:p.Pro4280His
|
|
XM_017009185.1:c.9023C>A
|
XP_016864674.1:p.Pro3008His
|
|
XM_017009186.1:c.8576C>A
|
XP_016864675.1:p.Pro2859His
|
|
XM_017009188.1:c.7913C>A
|
XP_016864677.1:p.Pro2638His
|
|
XM_024454388.1:c.12839C>A
|
XP_024310156.1:p.Pro4280His
|
|
XM_024454389.1:c.12428C>A
|
XP_024310157.1:p.Pro4143His
|
|
NM_001369.3:c.13826C>A
MANE Select
|
NP_001360.1:p.Pro4609His
|
|