ENST00000322776.11:c.700+2T>A
MANE Select
|
ENSP00000322450.6:n.700+2T>A
|
|
ENST00000647561.1:c.700+2T>A
|
ENSP00000497587.1:n.700+2T>A
|
|
ENST00000322776.10:c.700+2T>A
|
ENSP00000322450.6:n.700+2T>A
|
|
ENST00000415352.6:c.679+2T>A
|
ENSP00000395368.2:n.679+2T>A
|
|
ENST00000526169.1:n.442+2T>A
|
|
|
ENST00000526770.5:n.561T>A
|
|
|
ENST00000529927.5:c.673+2T>A
|
ENSP00000436766.1:n.673+2T>A
|
|
ENST00000532244.5:c.399T>A
|
ENSP00000435202.1:p.Gly133=
|
|
ENST00000532303.5:c.397+2T>A
|
ENSP00000432015.1:n.397+2T>A
|
|
ENST00000533919.5:c.178+2T>A
|
ENSP00000435199.1:n.178+2T>A
|
|
NM_001166102.1:c.673+2T>A
|
NP_001159574.1:n.673+2T>A
|
|
NM_007103.3:c.700+2T>A
|
NP_009034.2:n.700+2T>A
|
|
NM_001166102.2:c.673+2T>A
|
NP_001159574.1:n.673+2T>A
|
|
NM_007103.4:c.700+2T>A
MANE Select
|
NP_009034.2:n.700+2T>A
|
|