ENST00000268314.9:c.1186G>C
MANE Select
|
ENSP00000268314.4:p.Gly396Arg
|
|
ENST00000268314.8:c.1186G>C
|
ENSP00000268314.4:p.Gly396Arg
|
|
ENST00000408912.7:c.1471G>C
|
ENSP00000386125.3:p.Gly491Arg
|
|
ENST00000457010.6:c.1186G>C
|
ENSP00000399561.2:p.Gly396Arg
|
|
ENST00000538189.5:c.694G>C
|
ENSP00000443995.2:p.Gly232Arg
|
|
ENST00000563544.5:c.1186G>C
|
ENSP00000456877.1:p.Gly396Arg
|
|
ENST00000564900.1:c.213-39G>C
|
|
|
NM_001105247.1:c.1186G>C
|
NP_001098717.1:p.Gly396Arg
|
|
NM_001288767.1:c.1471G>C
|
NP_001275696.1:p.Gly491Arg
|
|
NM_001301820.1:c.1282G>C
|
NP_001288749.1:p.Gly428Arg
|
|
NM_024742.2:c.1186G>C
|
NP_079018.1:p.Gly396Arg
|
|
XM_006721091.1:c.1282G>C
|
XP_006721154.1:p.Gly428Arg
|
|
XM_006721091.3:c.1282G>C
|
XP_006721154.1:p.Gly428Arg
|
|
XM_024450448.1:c.1282G>C
|
XP_024306216.1:p.Gly428Arg
|
|
XM_024450449.1:c.1282G>C
|
XP_024306217.1:p.Gly428Arg
|
|
NM_001105247.2:c.1186G>C
MANE Select
|
NP_001098717.1:p.Gly396Arg
|
|
NM_001288767.2:c.1471G>C
|
NP_001275696.1:p.Gly491Arg
|
|