ENST00000302068.9:c.1197T>C
MANE Select
|
ENSP00000306099.4:p.Ile399=
|
|
ENST00000302068.8:c.1197T>C
|
ENSP00000306099.4:p.Ile399=
|
|
ENST00000502545.5:n.939+445T>C
|
|
|
ENST00000509493.1:c.540T>C
|
ENSP00000426757.1:p.Ile180=
|
|
NM_001184741.1:c.1020T>C
|
NP_001171670.1:p.Ile340=
|
|
NM_005141.4:c.1197T>C , LRG_558t1:c.1197T>C
|
NP_005132.2:p.Ile399=
|
|
NM_001382759.1:c.1065T>C
|
NP_001369688.1:p.Ile355=
|
|
NM_001382760.1:c.1197T>C
|
NP_001369689.1:p.Ile399=
|
|
NM_001382761.1:c.1197T>C
|
NP_001369690.1:p.Ile399=
|
|
NM_001382762.1:c.897T>C
|
NP_001369691.1:p.Ile299=
|
|
NM_001382763.1:c.1188T>C
|
NP_001369692.1:p.Ile396=
|
|
NM_001382764.1:c.1081-21T>C
|
NP_001369693.1:n.1081-21T>C
|
|
NM_001382765.1:c.1197T>C
|
NP_001369694.1:p.Ile399=
|
|
NM_005141.5:c.1197T>C
MANE Select
|
NP_005132.2:p.Ile399=
|
|