ENST00000321612.8:c.2053-295T>C
MANE Select
|
ENSP00000370737.4:n.2053-295T>C
|
|
ENST00000638233.1:n.488-295T>C
|
|
|
ENST00000638661.1:c.253-295T>C
|
ENSP00000491369.1:n.253-295T>C
|
|
ENST00000638694.1:n.240-295T>C
|
|
|
ENST00000639318.1:c.253-295T>C
|
ENSP00000491932.1:n.253-295T>C
|
|
ENST00000639364.1:n.1753-295T>C
|
|
|
ENST00000639443.1:n.1621-295T>C
|
|
|
ENST00000639954.1:n.1761-295T>C
|
|
|
ENST00000640505.1:n.292-295T>C
|
|
|
ENST00000321612.6:c.2053-295T>C
|
ENSP00000370737.3:n.2053-295T>C
|
|
NM_000170.2:c.2053-295T>C , LRG_643t1:c.2053-295T>C
|
NP_000161.2:n.2053-295T>C
|
|
NM_000170.3:c.2053-295T>C
MANE Select
|
NP_000161.2:n.2053-295T>C
|
|