ENST00000324041.6:c.580G>C
MANE Select
|
ENSP00000326159.1:p.Gly194Arg
|
|
ENST00000324041.5:c.580G>C
|
ENSP00000326159.1:p.Gly194Arg
|
|
ENST00000431178.2:c.328+188G>C
|
ENSP00000399448.2:n.328+188G>C
|
|
ENST00000593885.1:c.*75G>C
|
ENSP00000469769.1:n.*75G>C
|
|
ENST00000596876.1:n.582G>C
|
|
|
ENST00000598305.5:c.*75G>C
|
ENSP00000469963.1:n.*75G>C
|
|
ENST00000599865.5:n.516G>C
|
|
|
ENST00000602148.1:c.592G>C
|
ENSP00000472091.1:n.592G>C
|
|
NM_001302961.1:c.295G>C
|
NP_001289890.1:p.Gly99Arg
|
|
NM_004917.4:c.580G>C
|
NP_004908.4:p.Gly194Arg
|
|
NR_126566.1:n.569G>C
|
|
|
XM_005259441.3:c.295G>C
|
XP_005259498.2:p.Gly99Arg
|
|
XM_011527545.1:c.*75G>C
|
XP_011525847.1:n.*75G>C
|
|
XM_011527546.1:c.475+188G>C
|
XP_011525848.1:n.475+188G>C
|
|
XM_011527547.1:c.433G>C
|
XP_011525849.1:p.Gly145Arg
|
|
XM_005259441.4:c.295G>C
|
XP_005259498.2:p.Gly99Arg
|
|
XM_011527545.3:c.*75G>C
|
XP_011525847.1:n.*75G>C
|
|
XM_011527546.2:c.475+188G>C
|
XP_011525848.1:n.475+188G>C
|
|
NM_001302961.2:c.295G>C
|
NP_001289890.1:p.Gly99Arg
|
|
NR_126566.2:n.569G>C
|
|
|
NM_004917.5:c.580G>C
MANE Select
|
NP_004908.4:p.Gly194Arg
|
|