ENST00000682422.1:n.774G>T
|
|
|
ENST00000682545.1:c.*199G>T
|
ENSP00000508402.1:n.*199G>T
|
|
ENST00000682887.1:c.1594G>T
|
ENSP00000506946.1:n.1594G>T
|
|
ENST00000683302.1:c.1124G>T
|
ENSP00000507885.1:p.Gly375Val
|
|
ENST00000683557.1:c.*25G>T
|
ENSP00000508029.1:n.*25G>T
|
|
ENST00000367282.6:c.1193G>T
MANE Select
|
ENSP00000356251.4:p.Gly398Val
|
|
ENST00000367282.5:c.1193G>T
|
ENSP00000356251.4:p.Gly398Val
|
|
NM_004767.3:c.1193G>T
|
NP_004758.3:p.Gly398Val
|
|
XM_011510158.1:c.632G>T
|
XP_011508460.1:p.Gly211Val
|
|
NM_004767.4:c.1193G>T
|
NP_004758.3:p.Gly398Val
|
|
XM_011510158.2:c.632G>T
|
XP_011508460.1:p.Gly211Val
|
|
NM_004767.5:c.1193G>T
MANE Select
|
NP_004758.3:p.Gly398Val
|
|