ENST00000703783.1:n.303C>A
|
|
|
ENST00000703785.1:n.384C>A
|
|
|
ENST00000262464.9:c.3519C>A
MANE Select
|
ENSP00000262464.4:p.Thr1173=
|
|
ENST00000262464.8:c.3519C>A
|
ENSP00000262464.4:p.Thr1173=
|
|
ENST00000507835.5:c.69C>A
|
ENSP00000426839.1:p.Thr23=
|
|
ENST00000508053.5:c.3519C>A
|
ENSP00000424571.1:p.Thr1173=
|
|
ENST00000508989.5:c.3420C>A
|
ENSP00000425596.1:p.Thr1140=
|
|
ENST00000619499.4:c.3516C>A
|
ENSP00000482132.1:p.Thr1172=
|
|
NM_001999.3:c.3519C>A
|
NP_001990.2:p.Thr1173=
|
|
XM_017009228.2:c.3366C>A
|
XP_016864717.1:p.Thr1122=
|
|
NM_001999.4:c.3519C>A
MANE Select
|
NP_001990.2:p.Thr1173=
|
|