ENST00000394867.9:n.586G>T
|
|
|
ENST00000687128.1:n.586G>T
|
|
|
ENST00000262948.10:c.147G>T
MANE Select
|
ENSP00000262948.4:p.Gln49His
|
|
ENST00000262948.9:c.147G>T
|
ENSP00000262948.3:p.Gln49His
|
|
ENST00000394867.8:c.-145G>T
|
ENSP00000378336.1:n.-145G>T
|
|
ENST00000599345.1:n.344G>T
|
|
|
NM_030662.3:c.147G>T , LRG_750t1:c.147G>T
|
NP_109587.1:p.Gln49His
|
|
XM_006722799.2:c.147G>T
|
XP_006722862.1:p.Gln49His
|
|
XM_017026989.1:c.147G>T
|
XP_016882478.1:p.Gln49His
|
|
XM_017026990.1:c.147G>T
|
XP_016882479.1:p.Gln49His
|
|
XM_017026991.1:c.147G>T
|
XP_016882480.1:p.Gln49His
|
|
NM_030662.4:c.147G>T
MANE Select
|
NP_109587.1:p.Gln49His
|
|