ENST00000264381.8:c.1797T>A
MANE Select
|
ENSP00000264381.3:p.Cys599Ter
|
|
ENST00000264381.7:c.1797T>A
|
ENSP00000264381.3:p.Cys599Ter
|
|
ENST00000479451.5:c.387T>A
|
ENSP00000418325.1:p.Cys129Ter
|
|
ENST00000482958.1:c.*303T>A
|
ENSP00000419804.1:n.*303T>A
|
|
ENST00000497011.5:c.*187T>A
|
ENSP00000419505.1:n.*187T>A
|
|
NM_000055.2:c.1797T>A
|
NP_000046.1:p.Cys599Ter
|
|
XM_005247685.1:c.1920T>A
|
XP_005247742.1:p.Cys640Ter
|
|
NM_000055.3:c.1797T>A
|
NP_000046.1:p.Cys599Ter
|
|
NR_137635.1:n.439T>A
|
|
|
NR_137636.1:n.2043T>A
|
|
|
NM_000055.4:c.1797T>A
MANE Select
|
NP_000046.1:p.Cys599Ter
|
|
NR_137635.2:n.390T>A
|
|
|
NR_137636.2:n.1994T>A
|
|
|