ENST00000252486.9:c.655C>T
MANE Select
|
ENSP00000252486.3:p.Gln219Ter
|
|
ENST00000252486.8:c.655C>T
|
ENSP00000252486.3:p.Gln219Ter
|
|
ENST00000425718.1:c.655C>T
|
ENSP00000410423.1:p.Gln219Ter
|
|
ENST00000434152.5:c.733C>T
|
ENSP00000413653.2:p.Gln245Ter
|
|
NM_000041.3:c.655C>T
|
NP_000032.1:p.Gln219Ter
|
|
NM_001302688.1:c.733C>T
|
NP_001289617.1:p.Gln245Ter
|
|
NM_001302689.1:c.655C>T
|
NP_001289618.1:p.Gln219Ter
|
|
NM_001302690.1:c.655C>T
|
NP_001289619.1:p.Gln219Ter
|
|
NM_001302691.1:c.655C>T
|
NP_001289620.1:p.Gln219Ter
|
|
NM_000041.4:c.655C>T
MANE Select
|
NP_000032.1:p.Gln219Ter
|
|
NM_001302688.2:c.733C>T
|
NP_001289617.1:p.Gln245Ter
|
|
NM_001302689.2:c.655C>T
|
NP_001289618.1:p.Gln219Ter
|
|
NM_001302691.2:c.655C>T
|
NP_001289620.1:p.Gln219Ter
|
|
NM_001302690.2:c.655C>T
|
NP_001289619.1:p.Gln219Ter
|
|