ENST00000318158.11:c.384G=
MANE Select
|
ENSP00000313432.6:p.Glu128=
|
|
ENST00000318158.10:c.384G=
|
ENSP00000313432.6:p.Glu128=
|
|
ENST00000377824.8:n.421G=
|
|
|
ENST00000460882.5:n.411G=
|
|
|
ENST00000487399.5:n.936G=
|
|
|
ENST00000491488.5:n.110-1850G=
|
|
|
ENST00000493368.5:n.441G=
|
|
|
ENST00000607784.1:c.384G=
|
ENSP00000475569.1:p.Glu128=
|
|
NM_012203.1:c.384G=
|
NP_036335.1:p.Glu128=
|
|
XM_005251631.1:c.84-1850G=
|
XP_005251688.1:n.84-1850G=
|
|
XM_011518073.1:c.-379G=
|
XP_011516375.1:n.-379G=
|
|
XR_929374.1:n.469G=
|
|
|
XM_017015320.2:c.384G=
|
XP_016870809.1:p.Glu128=
|
|
XM_017015321.2:c.384G=
|
XP_016870810.1:p.Glu128=
|
|
XM_017015323.2:c.-379G=
|
XP_016870812.1:n.-379G=
|
|
XM_024447716.1:c.657G=
|
XP_024303484.1:p.Glu219=
|
|
XM_024447717.1:c.657G=
|
XP_024303485.1:p.Glu219=
|
|
XR_002956828.1:n.672G=
|
|
|
XR_002956829.1:n.672G=
|
|
|
XR_002956830.1:n.443G=
|
|
|
XR_002956831.1:n.139-1850G=
|
|
|
XR_002956832.1:n.443G=
|
|
|
NM_012203.2:c.384G=
MANE Select
|
NP_036335.1:p.Glu128=
|
|