ENST00000452035.7:n.168T>C
|
|
|
ENST00000483004.2:c.-10T>C
|
ENSP00000419887.2:n.-10T>C
|
|
ENST00000497841.6:c.-10T>C
|
ENSP00000513847.1:n.-10T>C
|
|
ENST00000698628.1:c.-10T>C
|
ENSP00000513848.1:n.-10T>C
|
|
ENST00000698629.1:n.168T>C
|
|
|
ENST00000698630.1:n.152T>C
|
|
|
ENST00000698631.1:n.147T>C
|
|
|
ENST00000698632.1:n.119T>C
|
|
|
ENST00000698633.1:n.89T>C
|
|
|
ENST00000698636.1:n.213T>C
|
|
|
ENST00000425368.7:c.-10T>C
MANE Select
|
ENSP00000416561.2:n.-10T>C
|
|
ENST00000425368.6:c.-10T>C
|
ENSP00000416561.2:n.-10T>C
|
|
ENST00000456570.5:c.1571-161T>C
|
ENSP00000410815.1:n.1571-161T>C
|
|
ENST00000460718.5:c.-10T>C
|
ENSP00000417793.1:n.-10T>C
|
|
ENST00000472581.1:n.238T>C
|
|
|
ENST00000475617.5:c.-10T>C
|
ENSP00000420090.1:n.-10T>C
|
|
ENST00000477310.1:c.1352-795T>C
|
ENSP00000418996.1:n.1352-795T>C
|
|
NM_001710.5:c.-10T>C , LRG_136t1:c.-10T>C
|
NP_001701.2:n.-10T>C
|
|
NM_001710.6:c.-10T>C
MANE Select
|
NP_001701.2:n.-10T>C
|
|