ENST00000225964.10:c.4370A>G
MANE Select
|
ENSP00000225964.6:p.Asp1457Gly
|
|
ENST00000225964.9:c.4370A>G
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ENSP00000225964.5:p.Asp1457Gly
|
|
NM_000088.3:c.4370A>G , LRG_1t1:c.4370A>G
|
NP_000079.2:p.Asp1457Gly
|
|
XM_005257058.3:c.4100A>G
|
XP_005257115.2:p.Asp1367Gly
|
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XM_005257059.3:c.3452A>G
|
XP_005257116.2:p.Asp1151Gly
|
|
XM_011524341.1:c.4172A>G
|
XP_011522643.1:p.Asp1391Gly
|
|
XM_005257058.4:c.4100A>G
|
XP_005257115.2:p.Asp1367Gly
|
|
XM_005257059.4:c.3452A>G
|
XP_005257116.2:p.Asp1151Gly
|
|
NM_000088.4:c.4370A>G
MANE Select
|
NP_000079.2:p.Asp1457Gly
|
|