ENST00000697291.1:c.*2424G>C
|
ENSP00000513228.1:n.*2424G>C
|
|
ENST00000648433.1:c.2710G>C
|
ENSP00000496816.1:p.Glu904Gln
|
|
ENST00000649426.1:n.588G>C
|
|
|
ENST00000649554.1:n.2437G>C
|
|
|
ENST00000649979.2:c.2827G>C
MANE Select
|
ENSP00000497271.1:p.Glu943Gln
|
|
ENST00000679938.1:c.2515G>C
|
ENSP00000505518.1:p.Glu839Gln
|
|
ENST00000263642.2:c.2827G>C
|
ENSP00000263642.2:p.Glu943Gln
|
|
NM_022168.3:c.2827G>C
|
NP_071451.2:p.Glu943Gln
|
|
XM_011511628.1:c.2110G>C
|
XP_011509930.1:p.Glu704Gln
|
|
NM_022168.4:c.2827G>C
MANE Select
|
NP_071451.2:p.Glu943Gln
|
|