ENST00000262494.13:c.594G>C
|
ENSP00000262494.7:p.Arg198Ser
|
|
ENST00000262493.12:c.594G>C
MANE Select
|
ENSP00000262493.6:p.Arg198Ser
|
|
ENST00000262494.12:c.594G>C
|
ENSP00000262494.7:p.Arg198Ser
|
|
ENST00000562316.6:c.261G>C
|
ENSP00000457238.2:p.Arg87Ser
|
|
ENST00000638185.1:n.809G>C
|
|
|
ENST00000638210.1:n.894G>C
|
|
|
ENST00000638705.1:c.594G>C
|
ENSP00000491223.1:p.Arg198Ser
|
|
ENST00000638836.1:n.504G>C
|
|
|
ENST00000639055.1:n.1315G>C
|
|
|
ENST00000639251.1:n.495G>C
|
|
|
ENST00000639268.1:c.229G>C
|
|
|
ENST00000639341.1:c.119G>C
|
|
|
ENST00000639770.1:c.632G>C
|
ENSP00000491999.1:n.632G>C
|
|
ENST00000640390.1:n.524G>C
|
|
|
ENST00000640560.1:n.370G>C
|
|
|
ENST00000640893.1:c.433G>C
|
ENSP00000492677.1:p.Ala145Pro
|
|
ENST00000262493.10:c.594G>C
|
ENSP00000262493.6:p.Arg198Ser
|
|
ENST00000262494.11:c.594G>C
|
ENSP00000262494.7:p.Arg198Ser
|
|
NM_020988.2:c.594G>C
|
NP_066268.1:p.Arg198Ser
|
|
NM_138736.2:c.594G>C
|
NP_620073.2:p.Arg198Ser
|
|
XM_011523003.1:c.468G>C
|
XP_011521305.1:p.Arg156Ser
|
|
XM_011523003.3:c.468G>C
|
XP_011521305.1:p.Arg156Ser
|
|
NM_020988.3:c.594G>C
MANE Select
|
NP_066268.1:p.Arg198Ser
|
|
NM_138736.3:c.594G>C
|
NP_620073.2:p.Arg198Ser
|
|