ENST00000398603.6:c.337-185G>C
|
ENSP00000381604.1:n.337-185G>C
|
|
ENST00000398606.10:c.437G>C
MANE Select
|
ENSP00000381607.3:p.Gly146Ala
|
|
ENST00000646888.1:c.*153G>C
|
ENSP00000494477.1:n.*153G>C
|
|
ENST00000398603.5:c.337-185G>C
|
ENSP00000381604.1:n.337-185G>C
|
|
ENST00000398606.7:c.437G>C
|
ENSP00000381607.3:p.Gly146Ala
|
|
ENST00000467591.1:n.548G>C
|
|
|
ENST00000494593.1:n.1232G>C
|
|
|
ENST00000495996.1:c.101G>C
|
ENSP00000484686.1:p.Gly34Ala
|
|
ENST00000498765.5:c.500G>C
|
|
|
NM_000852.3:c.437G>C , LRG_723t1:c.437G>C
|
NP_000843.1:p.Gly146Ala
|
|
NM_000852.4:c.437G>C
MANE Select
|
NP_000843.1:p.Gly146Ala
|
|