ENST00000697291.1:c.*2408A>T
|
ENSP00000513228.1:n.*2408A>T
|
|
ENST00000648433.1:c.2694A>T
|
ENSP00000496816.1:p.Glu898Asp
|
|
ENST00000649426.1:n.572A>T
|
|
|
ENST00000649554.1:n.2421A>T
|
|
|
ENST00000649979.2:c.2811A>T
MANE Select
|
ENSP00000497271.1:p.Glu937Asp
|
|
ENST00000679938.1:c.2499A>T
|
ENSP00000505518.1:p.Glu833Asp
|
|
ENST00000263642.2:c.2811A>T
|
ENSP00000263642.2:p.Glu937Asp
|
|
NM_022168.3:c.2811A>T
|
NP_071451.2:p.Glu937Asp
|
|
XM_011511628.1:c.2094A>T
|
XP_011509930.1:p.Glu698Asp
|
|
NM_022168.4:c.2811A>T
MANE Select
|
NP_071451.2:p.Glu937Asp
|
|