ENST00000265316.9:c.1474G>A
(ABCB6)
MANE Select
|
ENSP00000265316.3:p.Ala492Thr
|
|
ENST00000295750.5:c.1336G>A
(ABCB6)
|
ENSP00000295750.5:p.Ala446Thr
|
|
ENST00000265316.7:c.1474G>A
(ABCB6)
|
ENSP00000265316.3:p.Ala492Thr
|
|
ENST00000295750.4:c.1017G>A
(ABCB6)
|
|
|
ENST00000446716.5:c.4199G>A
(ATG9A)
|
|
|
ENST00000448398.5:c.550G>A
(ABCB6)
|
|
|
ENST00000494639.5:n.383G>A
(ABCB6)
|
|
|
ENST00000496984.5:n.675G>A
(ABCB6)
|
|
|
ENST00000497882.5:n.1787G>A
(ABCB6)
|
|
|
NM_005689.2:c.1474G>A
(ABCB6)
|
NP_005680.1:p.Ala492Thr
|
|
NM_001349828.1:c.1336G>A
(ABCB6)
|
NP_001336757.1:p.Ala446Thr
|
|
NM_005689.3:c.1474G>A
(ABCB6)
|
NP_005680.1:p.Ala492Thr
|
|
NM_005689.4:c.1474G>A
(ABCB6)
MANE Select
|
NP_005680.1:p.Ala492Thr
|
|
NM_001349828.2:c.1336G>A
(ABCB6)
|
NP_001336757.1:p.Ala446Thr
|
|