ENST00000342245.9:c.1142C>T
MANE Select
|
ENSP00000340409.4:p.Ser381Phe
|
|
ENST00000342245.8:c.1142C>T
|
ENSP00000340409.4:p.Ser381Phe
|
|
ENST00000526280.1:c.321-351C>T
|
|
|
ENST00000527275.5:c.1139C>T
|
ENSP00000435350.1:p.Ser380Phe
|
|
ENST00000531303.5:c.489C>T
|
ENSP00000432625.1:p.Leu163=
|
|
ENST00000533123.5:c.1092-351C>T
|
ENSP00000435950.1:n.1092-351C>T
|
|
ENST00000534405.5:c.1182C>T
|
ENSP00000434353.1:p.Leu394=
|
|
NM_000543.4:c.1142C>T
|
NP_000534.3:p.Ser381Phe
|
|
NM_001007593.2:c.1139C>T
|
NP_001007594.2:p.Ser380Phe
|
|
XM_005253075.3:c.1142C>T
|
XP_005253132.1:p.Ser381Phe
|
|
XM_011520303.1:c.1132-351C>T
|
XP_011518605.1:n.1132-351C>T
|
|
XM_011520304.1:c.1132-351C>T
|
XP_011518606.1:n.1132-351C>T
|
|
XR_930886.1:n.1480C>T
|
|
|
NM_001318087.1:c.1142C>T
|
NP_001305016.1:p.Ser381Phe
|
|
NM_001318088.1:c.221C>T
|
NP_001305017.1:p.Ser74Phe
|
|
NM_001365135.1:c.1132-351C>T
|
NP_001352064.1:n.1132-351C>T
|
|
NR_027400.2:n.1277-351C>T
|
|
|
NR_134502.1:n.674C>T
|
|
|
XM_011520304.2:c.1132-351C>T
|
XP_011518606.1:n.1132-351C>T
|
|
XR_001747940.2:n.1307C>T
|
|
|
XR_002957158.1:n.1307C>T
|
|
|
NM_000543.5:c.1142C>T
MANE Select
|
NP_000534.3:p.Ser381Phe
|
|
NM_001007593.3:c.1139C>T
|
NP_001007594.2:p.Ser380Phe
|
|
NM_001318087.2:c.1142C>T
|
NP_001305016.1:p.Ser381Phe
|
|
NM_001318088.2:c.221C>T
|
NP_001305017.1:p.Ser74Phe
|
|
NM_001365135.2:c.1132-351C>T
|
NP_001352064.1:n.1132-351C>T
|
|
NR_027400.3:n.1217-351C>T
|
|
|
NR_134502.2:n.614C>T
|
|
|