ENST00000309755.9:c.1047G>C
MANE Select
|
ENSP00000312397.4:p.Val349=
|
|
ENST00000309755.8:c.1047G>C
|
ENSP00000312397.4:p.Val349=
|
|
ENST00000502381.1:n.634G>C
|
|
|
ENST00000504208.5:c.*335-10688G>C
|
ENSP00000423585.1:n.*335-10688G>C
|
|
ENST00000505853.1:c.927G>C
|
ENSP00000426173.1:p.Val309=
|
|
ENST00000506491.5:c.801G>C
|
ENSP00000424828.1:p.Val267=
|
|
ENST00000506873.5:n.672G>C
|
|
|
ENST00000508657.5:c.951G>C
|
ENSP00000422099.1:p.Val317=
|
|
NM_001257194.1:c.951G>C
|
NP_001244123.1:p.Val317=
|
|
NM_001257195.1:c.801G>C
|
NP_001244124.1:p.Val267=
|
|
NM_017415.2:c.1047G>C
|
NP_059111.2:p.Val349=
|
|
NM_017415.3:c.1047G>C
MANE Select
|
NP_059111.2:p.Val349=
|
|
NM_001257195.2:c.801G>C
|
NP_001244124.1:p.Val267=
|
|