ENST00000622290.5:c.*672A>G
|
ENSP00000483331.2:n.*672A>G
|
|
ENST00000205557.12:c.4500A>G
MANE Select
|
ENSP00000205557.7:p.Ser1500=
|
|
ENST00000640696.1:c.1314A>G
|
ENSP00000492197.1:p.Ser438=
|
|
ENST00000205557.11:c.4500A>G
|
ENSP00000205557.7:p.Ser1500=
|
|
ENST00000456970.6:c.4125A>G
|
ENSP00000405002.2:n.4125A>G
|
|
ENST00000576204.5:n.1363A>G
|
|
|
ENST00000622290.4:c.*1709A>G
|
ENSP00000483331.1:n.*1709A>G
|
|
NM_001171.5:c.4500A>G
|
NP_001162.4:p.Ser1500=
|
|
XM_011522479.1:c.4467A>G
|
XP_011520781.1:p.Ser1489=
|
|
XM_011522480.1:c.4158A>G
|
XP_011520782.1:p.Ser1386=
|
|
XM_011522481.1:c.4158A>G
|
XP_011520783.1:p.Ser1386=
|
|
XR_933134.1:n.538+5855T>C
|
|
|
NM_001351800.1:c.4158A>G
|
NP_001338729.1:p.Ser1386=
|
|
NR_147784.1:n.4162A>G
|
|
|
XM_011522479.2:c.4467A>G
|
XP_011520781.1:p.Ser1489=
|
|
XM_011522481.3:c.4158A>G
|
XP_011520783.1:p.Ser1386=
|
|
XM_017023212.1:c.4332A>G
|
XP_016878701.1:p.Ser1444=
|
|
XM_024450261.1:c.4536A>G
|
XP_024306029.1:p.Ser1512=
|
|
NM_001171.6:c.4500A>G
MANE Select
|
NP_001162.5:p.Ser1500=
|
|