ENST00000574094.6:c.1336C>T
|
ENSP00000507301.1:p.Gln446Ter
|
|
ENST00000622290.5:c.1336C>T
|
ENSP00000483331.2:p.Gln446Ter
|
|
ENST00000205557.12:c.1336C>T
MANE Select
|
ENSP00000205557.7:p.Gln446Ter
|
|
ENST00000205557.11:c.1336C>T
|
ENSP00000205557.7:p.Gln446Ter
|
|
ENST00000456970.6:c.1336C>T
|
ENSP00000405002.2:p.Gln446Ter
|
|
ENST00000574094.5:n.1432C>T
|
|
|
ENST00000622290.4:c.1336C>T
|
ENSP00000483331.1:p.Gln446Ter
|
|
NM_001171.5:c.1336C>T
|
NP_001162.4:p.Gln446Ter
|
|
XM_011522479.1:c.1336C>T
|
XP_011520781.1:p.Gln446Ter
|
|
XM_011522480.1:c.994C>T
|
XP_011520782.1:p.Gln332Ter
|
|
XM_011522481.1:c.994C>T
|
XP_011520783.1:p.Gln332Ter
|
|
XM_011522482.1:c.1336C>T
|
XP_011520784.1:p.Gln446Ter
|
|
XR_932836.1:n.1571C>T
|
|
|
XR_932837.1:n.1572C>T
|
|
|
XR_932838.1:n.1572C>T
|
|
|
NM_001351800.1:c.994C>T
|
NP_001338729.1:p.Gln332Ter
|
|
NR_147784.1:n.1373C>T
|
|
|
XM_011522479.2:c.1336C>T
|
XP_011520781.1:p.Gln446Ter
|
|
XM_011522481.3:c.994C>T
|
XP_011520783.1:p.Gln332Ter
|
|
XM_011522482.3:c.1336C>T
|
XP_011520784.1:p.Gln446Ter
|
|
XM_017023212.1:c.1336C>T
|
XP_016878701.1:p.Gln446Ter
|
|
XM_017023214.1:c.1336C>T
|
XP_016878703.1:p.Gln446Ter
|
|
XM_024450261.1:c.1372C>T
|
XP_024306029.1:p.Gln458Ter
|
|
XR_932836.2:n.1517C>T
|
|
|
XR_932837.3:n.1517C>T
|
|
|
XR_932838.3:n.1517C>T
|
|
|
NM_001171.6:c.1336C>T
MANE Select
|
NP_001162.5:p.Gln446Ter
|
|