ENST00000406870.7:c.-49-4014A>G
MANE Select
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ENSP00000384371.2:n.-49-4014A>G
|
|
ENST00000406870.6:c.-49-4014A>G
|
ENSP00000384371.2:n.-49-4014A>G
|
|
ENST00000470319.1:n.64-4014A>G
|
|
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ENST00000480458.5:n.29-4014A>G
|
|
|
ENST00000496823.1:n.51-1647A>G
|
|
|
ENST00000621333.4:c.-49-4014A>G
|
ENSP00000479784.1:n.-49-4014A>G
|
|
NM_001706.4:c.-49-4014A>G
|
NP_001697.2:n.-49-4014A>G
|
|
XM_005247694.2:c.-1374A>G
|
XP_005247751.1:n.-1374A>G
|
|
XM_011513062.1:c.-49-4014A>G
|
XP_011511364.1:n.-49-4014A>G
|
|
XM_005247694.4:c.-1374A>G
|
XP_005247751.1:n.-1374A>G
|
|
XM_011513062.3:c.-49-4014A>G
|
XP_011511364.1:n.-49-4014A>G
|
|
NM_001706.5:c.-49-4014A>G
MANE Select
|
NP_001697.2:n.-49-4014A>G
|
|