ENST00000696512.1:c.3100C>A
|
ENSP00000512678.1:p.Arg1034=
|
|
ENST00000394412.8:c.2977C>A
MANE Select
|
ENSP00000377934.3:p.Arg993=
|
|
ENST00000677187.1:n.651C>A
|
|
|
ENST00000394412.7:c.2977C>A
|
ENSP00000377934.3:p.Arg993=
|
|
NM_198525.2:c.2977C>A
|
NP_940927.2:p.Arg993=
|
|
XM_005254902.2:c.2977C>A
|
XP_005254959.1:p.Arg993=
|
|
XM_011521531.1:c.3100C>A
|
XP_011519833.1:p.Arg1034=
|
|
XM_011521532.1:c.3097C>A
|
XP_011519834.1:p.Arg1033=
|
|
XM_011521533.1:c.3097C>A
|
XP_011519835.1:p.Arg1033=
|
|
XM_011521534.1:c.3100C>A
|
XP_011519836.1:p.Arg1034=
|
|
XM_011521535.1:c.3100C>A
|
XP_011519837.1:p.Arg1034=
|
|
XM_011521536.1:c.3100C>A
|
XP_011519838.1:p.Arg1034=
|
|
XM_011521531.2:c.3100C>A
|
XP_011519833.1:p.Arg1034=
|
|
NM_198525.3:c.2977C>A
MANE Select
|
NP_940927.2:p.Arg993=
|
|