ENST00000310373.7:c.773C>T
(GP6)
|
ENSP00000308782.3:p.Ala258Val
|
|
ENST00000333884.2:c.719C>T
(GP6)
|
ENSP00000334552.2:p.Ala240Val
|
|
ENST00000417454.5:c.773C>T
(GP6)
MANE Select
|
ENSP00000394922.1:p.Ala258Val
|
|
ENST00000465648.1:n.217C>T
(GP6)
|
|
|
NM_001083899.2:c.773C>T , LRG_560t3:c.773C>T
(GP6)
|
NP_001077368.2:p.Ala258Val
|
|
NM_001256017.2:c.719C>T , LRG_560t2:c.719C>T
(GP6)
|
NP_001242946.2:p.Ala240Val
|
|
NM_016363.5:c.773C>T , LRG_560t1:c.773C>T
(GP6)
MANE Select
|
NP_057447.5:p.Ala258Val
|
|
XR_001754012.2:n.312+9221G>A
(GP6-AS1)
|
|
|
XR_001754013.2:n.305+9221G>A
(GP6-AS1)
|
|
|