ENST00000703783.1:n.497A>T
|
|
|
ENST00000703785.1:n.578A>T
|
|
|
ENST00000262464.9:c.3713A>T
MANE Select
|
ENSP00000262464.4:p.Gln1238Leu
|
|
ENST00000262464.8:c.3713A>T
|
ENSP00000262464.4:p.Gln1238Leu
|
|
ENST00000507835.5:c.263A>T
|
ENSP00000426839.1:p.Gln88Leu
|
|
ENST00000508053.5:c.3713A>T
|
ENSP00000424571.1:p.Gln1238Leu
|
|
ENST00000508989.5:c.3614A>T
|
ENSP00000425596.1:p.Gln1205Leu
|
|
ENST00000619499.4:c.3710A>T
|
ENSP00000482132.1:p.Gln1237Leu
|
|
NM_001999.3:c.3713A>T
|
NP_001990.2:p.Gln1238Leu
|
|
XM_017009228.2:c.3560A>T
|
XP_016864717.1:p.Gln1187Leu
|
|
NM_001999.4:c.3713A>T
MANE Select
|
NP_001990.2:p.Gln1238Leu
|
|