ENST00000324856.13:c.5311C>G
MANE Select
|
ENSP00000320485.7:p.Pro1771Ala
|
|
ENST00000374152.7:c.4162C>G
|
ENSP00000363267.2:p.Pro1388Ala
|
|
ENST00000430799.7:c.4159C>G
|
ENSP00000390317.3:p.Pro1387Ala
|
|
ENST00000466382.2:c.728C>G
|
|
|
ENST00000636219.1:c.4165C>G
|
ENSP00000489842.1:p.Pro1389Ala
|
|
ENST00000637788.1:n.1111C>G
|
|
|
ENST00000324856.11:c.5311C>G
|
ENSP00000320485.7:p.Pro1771Ala
|
|
ENST00000374152.6:c.4162C>G
|
ENSP00000363267.2:p.Pro1388Ala
|
|
ENST00000430799.6:c.2000C>G
|
|
|
ENST00000457599.6:c.4660C>G
|
ENSP00000387636.2:p.Pro1554Ala
|
|
ENST00000466382.1:c.728C>G
|
|
|
ENST00000532781.1:c.809C>G
|
|
|
NM_006015.4:c.5311C>G , LRG_875t1:c.5311C>G
|
NP_006006.3:p.Pro1771Ala
|
|
NM_139135.2:c.4660C>G
|
NP_624361.1:p.Pro1554Ala
|
|
NM_006015.5:c.5311C>G
|
NP_006006.3:p.Pro1771Ala
|
|
NM_139135.3:c.4660C>G
|
NP_624361.1:p.Pro1554Ala
|
|
NM_006015.6:c.5311C>G
MANE Select
|
NP_006006.3:p.Pro1771Ala
|
|
NM_139135.4:c.4660C>G
|
NP_624361.1:p.Pro1554Ala
|
|