ENST00000315491.12:c.1336G>T
MANE Select
|
ENSP00000320295.7:p.Ala446Ser
|
|
ENST00000680788.1:n.4757G>T
|
|
|
ENST00000315491.11:c.1336G>T
|
ENSP00000320295.7:p.Ala446Ser
|
|
ENST00000554444.5:c.1120G>T
|
ENSP00000451617.1:p.Ala374Ser
|
|
ENST00000555576.5:c.277+2209G>T
|
ENSP00000452554.1:n.277+2209G>T
|
|
ENST00000555609.5:c.*1421G>T
|
ENSP00000451276.1:n.*1421G>T
|
|
ENST00000556922.1:c.2377G>T
|
ENSP00000451560.1:p.Ala793Ser
|
|
NM_001197181.1:c.1120G>T
|
NP_001184110.1:p.Ala374Ser
|
|
NM_006086.3:c.1336G>T
|
NP_006077.2:p.Ala446Ser
|
|
NM_006086.4:c.1336G>T
MANE Select
|
NP_006077.2:p.Ala446Ser
|
|
NM_001197181.2:c.1120G>T
|
NP_001184110.1:p.Ala374Ser
|
|