ENST00000651671.1:c.6038A>G
MANE Select
|
ENSP00000498587.1:p.Asp2013Gly
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ENST00000679595.1:c.*1078A>G
|
ENSP00000506241.1:n.*1078A>G
|
|
ENST00000679969.1:n.2519A>G
|
|
|
ENST00000680003.1:n.2370A>G
|
|
|
ENST00000680133.1:c.5924A>G
|
ENSP00000505319.1:p.Asp1975Gly
|
|
ENST00000680218.1:c.5918A>G
|
ENSP00000505339.1:p.Asp1973Gly
|
|
ENST00000680668.1:c.5924A>G
|
ENSP00000506336.1:p.Asp1975Gly
|
|
ENST00000680778.1:c.3635A>G
|
ENSP00000506033.1:p.Asp1212Gly
|
|
ENST00000680924.1:c.*3438A>G
|
ENSP00000506031.1:n.*3438A>G
|
|
ENST00000681135.1:c.*3647A>G
|
ENSP00000506636.1:n.*3647A>G
|
|
ENST00000681298.1:n.4143A>G
|
|
|
ENST00000681454.1:c.*5274A>G
|
ENSP00000505763.1:n.*5274A>G
|
|
ENST00000277541.6:c.6038A>G
|
ENSP00000277541.6:p.Asp2013Gly
|
|
NM_017617.3:c.6038A>G
|
NP_060087.3:p.Asp2013Gly
|
|
XM_011518717.1:c.5339A>G
|
XP_011517019.1:p.Asp1780Gly
|
|
NM_017617.5:c.6038A>G
MANE Select
|
NP_060087.3:p.Asp2013Gly
|
|
XM_011518717.2:c.5315A>G
|
XP_011517019.2:p.Asp1772Gly
|
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