ENST00000576204.6:n.778G>A
|
|
|
ENST00000622290.5:c.*87G>A
|
ENSP00000483331.2:n.*87G>A
|
|
ENST00000205557.12:c.3915G>A
MANE Select
|
ENSP00000205557.7:p.Lys1305=
|
|
ENST00000640696.1:c.729G>A
|
ENSP00000492197.1:p.Lys243=
|
|
ENST00000205557.11:c.3915G>A
|
ENSP00000205557.7:p.Lys1305=
|
|
ENST00000456970.6:c.3540G>A
|
ENSP00000405002.2:n.3540G>A
|
|
ENST00000576204.5:n.778G>A
|
|
|
ENST00000622290.4:c.*1124G>A
|
ENSP00000483331.1:n.*1124G>A
|
|
NM_001171.5:c.3915G>A
|
NP_001162.4:p.Lys1305=
|
|
XM_011522479.1:c.3882G>A
|
XP_011520781.1:p.Lys1294=
|
|
XM_011522480.1:c.3573G>A
|
XP_011520782.1:p.Lys1191=
|
|
XM_011522481.1:c.3573G>A
|
XP_011520783.1:p.Lys1191=
|
|
XR_932836.1:n.4213G>A
|
|
|
XR_932837.1:n.3951G>A
|
|
|
XR_932838.1:n.4014G>A
|
|
|
XR_933134.1:n.539-4782C>T
|
|
|
NM_001351800.1:c.3573G>A
|
NP_001338729.1:p.Lys1191=
|
|
NR_147784.1:n.3577G>A
|
|
|
XM_011522479.2:c.3882G>A
|
XP_011520781.1:p.Lys1294=
|
|
XM_011522481.3:c.3573G>A
|
XP_011520783.1:p.Lys1191=
|
|
XM_017023212.1:c.3747G>A
|
XP_016878701.1:p.Lys1249=
|
|
XM_024450261.1:c.3951G>A
|
XP_024306029.1:p.Lys1317=
|
|
XR_932836.2:n.4159G>A
|
|
|
XR_932837.3:n.3896G>A
|
|
|
XR_932838.3:n.3959G>A
|
|
|
NM_001171.6:c.3915G>A
MANE Select
|
NP_001162.5:p.Lys1305=
|
|