ENST00000452035.7:n.2303G>C
|
|
|
ENST00000483004.2:c.1600G>C
|
ENSP00000419887.2:p.Ala534Pro
|
|
ENST00000698628.1:c.1625-239G>C
|
ENSP00000513848.1:n.1625-239G>C
|
|
ENST00000698629.1:n.2088G>C
|
|
|
ENST00000698630.1:n.2532G>C
|
|
|
ENST00000698631.1:n.2533G>C
|
|
|
ENST00000698632.1:n.3422G>C
|
|
|
ENST00000698633.1:n.3312G>C
|
|
|
ENST00000425368.7:c.1816G>C
MANE Select
|
ENSP00000416561.2:p.Ala606Pro
|
|
ENST00000425368.6:c.1816G>C
|
ENSP00000416561.2:p.Ala606Pro
|
|
ENST00000456570.5:c.3322G>C
|
ENSP00000410815.1:p.Ala1108Pro
|
|
ENST00000467360.1:n.942G>C
|
|
|
ENST00000477310.1:c.2869G>C
|
ENSP00000418996.1:p.Ala957Pro
|
|
ENST00000482312.1:n.32G>C
|
|
|
ENST00000483004.1:c.438G>C
|
|
|
NM_001710.5:c.1816G>C , LRG_136t1:c.1816G>C
|
NP_001701.2:p.Ala606Pro
|
|
NM_001710.6:c.1816G>C
MANE Select
|
NP_001701.2:p.Ala606Pro
|
|