ENST00000367435.5:c.1009G>C
MANE Select
|
ENSP00000356405.4:p.Ala337Pro
|
|
ENST00000635846.1:c.766G>C
|
ENSP00000490035.1:p.Ala256Pro
|
|
ENST00000643006.1:c.1077G>C
|
ENSP00000496633.1:p.Gln359His
|
|
ENST00000648071.1:c.*985G>C
|
ENSP00000497513.1:n.*985G>C
|
|
ENST00000649613.1:n.259G>C
|
|
|
ENST00000649895.1:n.1227G>C
|
|
|
ENST00000650197.1:c.1009G>C
|
ENSP00000496929.1:p.Ala337Pro
|
|
ENST00000367435.3:c.1009G>C
|
ENSP00000356405.3:p.Ala337Pro
|
|
NM_024529.4:c.1009G>C , LRG_507t1:c.1009G>C
|
NP_078805.3:p.Ala337Pro
|
|
NM_024529.5:c.1009G>C
MANE Select
|
NP_078805.3:p.Ala337Pro
|
|