ENST00000394817.7:c.1345C>T
MANE Select
|
ENSP00000378294.2:p.Leu449=
|
|
ENST00000265195.9:c.1345C>T
|
ENSP00000265195.5:p.Leu449=
|
|
ENST00000394817.6:c.1345C>T
|
ENSP00000378294.2:p.Leu449=
|
|
ENST00000509534.5:c.1366C>T
|
ENSP00000426858.1:p.Leu456=
|
|
ENST00000515008.1:n.680C>T
|
|
|
NM_001037633.1:c.1345C>T
|
NP_001032722.1:p.Leu449=
|
|
NM_022464.4:c.1345C>T
|
NP_071909.1:p.Leu449=
|
|
XM_011543570.1:c.1375C>T
|
XP_011541872.1:p.Leu459=
|
|
XM_011543570.2:c.1375C>T
|
XP_011541872.1:p.Leu459=
|
|
XM_024446164.1:c.1345C>T
|
XP_024301932.1:p.Leu449=
|
|
NM_022464.5:c.1345C>T
MANE Select
|
NP_071909.1:p.Leu449=
|
|
NM_001037633.2:c.1345C>T
|
NP_001032722.1:p.Leu449=
|
|