ENST00000265316.9:c.2073T>C
(ABCB6)
MANE Select
|
ENSP00000265316.3:p.Ala691=
|
|
ENST00000295750.5:c.1935T>C
(ABCB6)
|
ENSP00000295750.5:p.Ala645=
|
|
ENST00000265316.7:c.2073T>C
(ABCB6)
|
ENSP00000265316.3:p.Ala691=
|
|
ENST00000295750.4:c.1616T>C
(ABCB6)
|
|
|
ENST00000443805.1:c.35T>C
(ABCB6)
|
|
|
ENST00000446716.5:c.4694-181T>C
(ATG9A)
|
|
|
ENST00000485773.5:n.105T>C
(ABCB6)
|
|
|
ENST00000487380.5:n.36T>C
(ABCB6)
|
|
|
ENST00000492543.1:n.623T>C
(ABCB6)
|
|
|
ENST00000497882.5:n.2386T>C
(ABCB6)
|
|
|
NM_005689.2:c.2073T>C
(ABCB6)
|
NP_005680.1:p.Ala691=
|
|
NM_001349828.1:c.1935T>C
(ABCB6)
|
NP_001336757.1:p.Ala645=
|
|
NM_005689.3:c.2073T>C
(ABCB6)
|
NP_005680.1:p.Ala691=
|
|
NM_005689.4:c.2073T>C
(ABCB6)
MANE Select
|
NP_005680.1:p.Ala691=
|
|
NM_001349828.2:c.1935T>C
(ABCB6)
|
NP_001336757.1:p.Ala645=
|
|