ENST00000682422.1:n.920G>T
|
|
|
ENST00000682545.1:c.*345G>T
|
ENSP00000508402.1:n.*345G>T
|
|
ENST00000682887.1:c.1740G>T
|
ENSP00000506946.1:n.1740G>T
|
|
ENST00000683302.1:c.1270G>T
|
ENSP00000507885.1:p.Ala424Ser
|
|
ENST00000683557.1:c.*171G>T
|
ENSP00000508029.1:n.*171G>T
|
|
ENST00000367282.6:c.1339G>T
MANE Select
|
ENSP00000356251.4:p.Ala447Ser
|
|
ENST00000367282.5:c.1339G>T
|
ENSP00000356251.4:p.Ala447Ser
|
|
NM_004767.3:c.1339G>T
|
NP_004758.3:p.Ala447Ser
|
|
XM_011510158.1:c.778G>T
|
XP_011508460.1:p.Ala260Ser
|
|
NM_004767.4:c.1339G>T
|
NP_004758.3:p.Ala447Ser
|
|
XM_011510158.2:c.778G>T
|
XP_011508460.1:p.Ala260Ser
|
|
NM_004767.5:c.1339G>T
MANE Select
|
NP_004758.3:p.Ala447Ser
|
|