ENST00000644269.2:c.1449G>A
MANE Select
|
ENSP00000494017.1:p.Val483=
|
|
ENST00000644846.1:c.160G>A
|
|
|
ENST00000265715.7:c.1449G>A
|
ENSP00000265715.3:p.Val483=
|
|
ENST00000460748.1:n.552G>A
|
|
|
ENST00000477350.5:n.296G>A
|
|
|
ENST00000480841.5:n.298G>A
|
|
|
ENST00000497446.5:n.464G>A
|
|
|
NM_000441.1:c.1449G>A
|
NP_000432.1:p.Val483=
|
|
XM_005250425.1:c.1449G>A
|
XP_005250482.1:p.Val483=
|
|
XM_005250425.2:c.1449G>A
|
XP_005250482.1:p.Val483=
|
|
XM_017012318.1:c.1371G>A
|
XP_016867807.1:p.Val457=
|
|
NM_000441.2:c.1449G>A
MANE Select
|
NP_000432.1:p.Val483=
|
|