ENST00000316407.9:c.*3833A>G
MANE Select
|
ENSP00000320794.4:n.*3833A>G
|
|
ENST00000316407.8:c.*3833A>G
|
ENSP00000320794.4:n.*3833A>G
|
|
ENST00000491165.5:c.257-1261A>G
|
ENSP00000420752.1:n.257-1261A>G
|
|
NM_001009899.3:c.*3833A>G
|
NP_001009899.3:n.*3833A>G
|
|
NR_111981.1:n.668-1261A>G
|
|
|
XM_005247208.3:c.*3833A>G
|
XP_005247265.2:n.*3833A>G
|
|
XM_005247208.4:c.*3833A>G
|
XP_005247265.2:n.*3833A>G
|
|
XM_017005871.1:c.*3833A>G
|
XP_016861360.1:n.*3833A>G
|
|
XM_017005872.1:c.*3833A>G
|
XP_016861361.1:n.*3833A>G
|
|
XM_024453391.1:c.*3833A>G
|
XP_024309159.1:n.*3833A>G
|
|
XM_024453392.1:c.*3833A>G
|
XP_024309160.1:n.*3833A>G
|
|
NM_001009899.4:c.*3833A>G
MANE Select
|
NP_001009899.3:n.*3833A>G
|
|
NR_111981.2:n.664-1261A>G
|
|
|