ENST00000452035.7:n.2173G=
|
|
|
ENST00000483004.2:c.1562+3G=
|
ENSP00000419887.2:n.1562+3G=
|
|
ENST00000698628.1:c.1625-369G=
|
ENSP00000513848.1:n.1625-369G=
|
|
ENST00000698629.1:n.1958G=
|
|
|
ENST00000698630.1:n.2494+3G=
|
|
|
ENST00000698631.1:n.2495+3G=
|
|
|
ENST00000698632.1:n.3292G=
|
|
|
ENST00000698633.1:n.3182G=
|
|
|
ENST00000698636.1:n.2003G=
|
|
|
ENST00000425368.7:c.1778+3G=
MANE Select
|
ENSP00000416561.2:n.1778+3G=
|
|
ENST00000425368.6:c.1778+3G=
|
ENSP00000416561.2:n.1778+3G=
|
|
ENST00000456570.5:c.3284+3G=
|
ENSP00000410815.1:n.3284+3G=
|
|
ENST00000467360.1:n.904+3G=
|
|
|
ENST00000477310.1:c.2831+3G=
|
ENSP00000418996.1:n.2831+3G=
|
|
ENST00000483004.1:c.400+3G=
|
|
|
NM_001710.5:c.1778+3G= , LRG_136t1:c.1778+3G=
|
NP_001701.2:n.1778+3G=
|
|
NM_001710.6:c.1778+3G=
MANE Select
|
NP_001701.2:n.1778+3G=
|
|