ENST00000315491.12:c.690G>T
MANE Select
|
ENSP00000320295.7:p.Ser230=
|
|
ENST00000680788.1:n.4111G>T
|
|
|
ENST00000315491.11:c.690G>T
|
ENSP00000320295.7:p.Ser230=
|
|
ENST00000554444.5:c.474G>T
|
ENSP00000451617.1:p.Ser158=
|
|
ENST00000555576.5:c.277+1563G>T
|
ENSP00000452554.1:n.277+1563G>T
|
|
ENST00000555609.5:c.*775G>T
|
ENSP00000451276.1:n.*775G>T
|
|
ENST00000555810.5:c.474G>T
|
ENSP00000450538.1:p.Ser158=
|
|
ENST00000556922.1:c.1731G>T
|
ENSP00000451560.1:p.Ser577=
|
|
NM_001197181.1:c.474G>T
|
NP_001184110.1:p.Ser158=
|
|
NM_006086.3:c.690G>T
|
NP_006077.2:p.Ser230=
|
|
NM_006086.4:c.690G>T
MANE Select
|
NP_006077.2:p.Ser230=
|
|
NM_001197181.2:c.474G>T
|
NP_001184110.1:p.Ser158=
|
|