ENST00000703783.1:n.271G>C
|
|
|
ENST00000703785.1:n.352G>C
|
|
|
ENST00000262464.9:c.3487G>C
MANE Select
|
ENSP00000262464.4:p.Glu1163Gln
|
|
ENST00000262464.8:c.3487G>C
|
ENSP00000262464.4:p.Glu1163Gln
|
|
ENST00000507835.5:c.37G>C
|
ENSP00000426839.1:p.Glu13Gln
|
|
ENST00000508053.5:c.3487G>C
|
ENSP00000424571.1:p.Glu1163Gln
|
|
ENST00000508989.5:c.3388G>C
|
ENSP00000425596.1:p.Glu1130Gln
|
|
ENST00000619499.4:c.3484G>C
|
ENSP00000482132.1:p.Glu1162Gln
|
|
NM_001999.3:c.3487G>C
|
NP_001990.2:p.Glu1163Gln
|
|
XM_017009228.2:c.3334G>C
|
XP_016864717.1:p.Glu1112Gln
|
|
NM_001999.4:c.3487G>C
MANE Select
|
NP_001990.2:p.Glu1163Gln
|
|