ENST00000315491.12:c.687A=
MANE Select
|
ENSP00000320295.7:p.Val229=
|
|
ENST00000680788.1:n.4108A=
|
|
|
ENST00000315491.11:c.687A=
|
ENSP00000320295.7:p.Val229=
|
|
ENST00000554444.5:c.471A=
|
ENSP00000451617.1:p.Val157=
|
|
ENST00000555576.5:c.277+1560A=
|
ENSP00000452554.1:n.277+1560A=
|
|
ENST00000555609.5:c.*772A=
|
ENSP00000451276.1:n.*772A=
|
|
ENST00000555810.5:c.471A=
|
ENSP00000450538.1:p.Val157=
|
|
ENST00000556922.1:c.1728A=
|
ENSP00000451560.1:p.Val576=
|
|
NM_001197181.1:c.471A=
|
NP_001184110.1:p.Val157=
|
|
NM_006086.3:c.687A=
|
NP_006077.2:p.Val229=
|
|
NM_006086.4:c.687A=
MANE Select
|
NP_006077.2:p.Val229=
|
|
NM_001197181.2:c.471A=
|
NP_001184110.1:p.Val157=
|
|