ENST00000315491.12:c.1257G>T
MANE Select
|
ENSP00000320295.7:p.Val419=
|
|
ENST00000680788.1:n.4678G>T
|
|
|
ENST00000315491.11:c.1257G>T
|
ENSP00000320295.7:p.Val419=
|
|
ENST00000554444.5:c.1041G>T
|
ENSP00000451617.1:p.Val347=
|
|
ENST00000555576.5:c.277+2130G>T
|
ENSP00000452554.1:n.277+2130G>T
|
|
ENST00000555609.5:c.*1342G>T
|
ENSP00000451276.1:n.*1342G>T
|
|
ENST00000556922.1:c.2298G>T
|
ENSP00000451560.1:p.Val766=
|
|
NM_001197181.1:c.1041G>T
|
NP_001184110.1:p.Val347=
|
|
NM_006086.3:c.1257G>T
|
NP_006077.2:p.Val419=
|
|
NM_006086.4:c.1257G>T
MANE Select
|
NP_006077.2:p.Val419=
|
|
NM_001197181.2:c.1041G>T
|
NP_001184110.1:p.Val347=
|
|