ENST00000683611.1:n.1182G>A
|
|
|
ENST00000265104.5:c.13849G>A
MANE Select
|
ENSP00000265104.4:p.Val4617Ile
|
|
ENST00000681290.1:c.13804G>A
|
ENSP00000505288.1:p.Val4602Ile
|
|
ENST00000265104.4:c.13849G>A
|
ENSP00000265104.4:p.Val4617Ile
|
|
NM_001369.2:c.13849G>A
|
NP_001360.1:p.Val4617Ile
|
|
XM_005248262.2:c.13804G>A
|
XP_005248319.1:p.Val4602Ile
|
|
XM_005248262.3:c.13957G>A
|
XP_005248319.2:p.Val4653Ile
|
|
XM_017009177.1:c.13537G>A
|
XP_016864666.1:p.Val4513Ile
|
|
XM_017009178.1:c.12862G>A
|
XP_016864667.1:p.Val4288Ile
|
|
XM_017009179.2:c.12862G>A
|
XP_016864668.1:p.Val4288Ile
|
|
XM_017009185.1:c.9046G>A
|
XP_016864674.1:p.Val3016Ile
|
|
XM_017009186.1:c.8599G>A
|
XP_016864675.1:p.Val2867Ile
|
|
XM_017009188.1:c.7936G>A
|
XP_016864677.1:p.Val2646Ile
|
|
XM_024454388.1:c.12862G>A
|
XP_024310156.1:p.Val4288Ile
|
|
XM_024454389.1:c.12451G>A
|
XP_024310157.1:p.Val4151Ile
|
|
NM_001369.3:c.13849G>A
MANE Select
|
NP_001360.1:p.Val4617Ile
|
|