ENST00000400521.7:c.1137G>T
MANE Select
|
ENSP00000383365.1:p.Val379=
|
|
ENST00000400518.5:c.1047G>T
|
ENSP00000383362.1:p.Val349=
|
|
ENST00000400519.6:c.1134G>T
|
ENSP00000383363.1:p.Val378=
|
|
ENST00000400521.6:c.1137G>T
|
ENSP00000383365.1:p.Val379=
|
|
ENST00000400525.6:c.1068G>T
|
ENSP00000383369.3:p.Val356=
|
|
ENST00000462330.5:c.60G>T
|
ENSP00000485603.2:p.Val20=
|
|
ENST00000462843.2:c.87G>T
|
ENSP00000485466.2:p.Val29=
|
|
ENST00000474308.5:c.1080G>T
|
ENSP00000485665.1:p.Val360=
|
|
ENST00000485358.5:c.105G>T
|
ENSP00000485499.2:p.Val35=
|
|
ENST00000487165.5:n.1231G>T
|
|
|
ENST00000494454.5:n.1211G>T
|
|
|
ENST00000495655.2:n.681G>T
|
|
|
ENST00000542719.6:c.849G>T
|
ENSP00000485128.2:p.Val283=
|
|
ENST00000634471.1:n.244-396G>T
|
|
|
ENST00000634537.1:c.366G>T
|
ENSP00000489208.1:p.Val122=
|
|
NM_006440.4:c.1137G>T
|
NP_006431.2:p.Val379=
|
|
NM_001352300.1:c.1134G>T
|
NP_001339229.1:p.Val378=
|
|
NM_001352301.1:c.1047G>T
|
NP_001339230.1:p.Val349=
|
|
NM_001352302.1:c.849G>T
|
NP_001339231.1:p.Val283=
|
|
NR_147957.1:n.1269G>T
|
|
|
NM_006440.5:c.1137G>T
MANE Select
|
NP_006431.2:p.Val379=
|
|
NM_001352300.2:c.1134G>T
|
NP_001339229.1:p.Val378=
|
|
NR_147957.2:n.1095G>T
|
|
|
NM_001352301.2:c.1047G>T
|
NP_001339230.1:p.Val349=
|
|
NM_001352302.2:c.849G>T
|
NP_001339231.1:p.Val283=
|
|