ENST00000682422.1:n.865G>C
|
|
|
ENST00000682545.1:c.*290G>C
|
ENSP00000508402.1:n.*290G>C
|
|
ENST00000682887.1:c.1685G>C
|
ENSP00000506946.1:n.1685G>C
|
|
ENST00000683302.1:c.1215G>C
|
ENSP00000507885.1:p.Leu405=
|
|
ENST00000683557.1:c.*116G>C
|
ENSP00000508029.1:n.*116G>C
|
|
ENST00000367282.6:c.1284G>C
MANE Select
|
ENSP00000356251.4:p.Leu428=
|
|
ENST00000367282.5:c.1284G>C
|
ENSP00000356251.4:p.Leu428=
|
|
NM_004767.3:c.1284G>C
|
NP_004758.3:p.Leu428=
|
|
XM_011510158.1:c.723G>C
|
XP_011508460.1:p.Leu241=
|
|
NM_004767.4:c.1284G>C
|
NP_004758.3:p.Leu428=
|
|
XM_011510158.2:c.723G>C
|
XP_011508460.1:p.Leu241=
|
|
NM_004767.5:c.1284G>C
MANE Select
|
NP_004758.3:p.Leu428=
|
|