ENST00000225964.10:c.3170T>G
MANE Select
|
ENSP00000225964.6:p.Val1057Gly
|
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ENST00000225964.9:c.3170T>G
|
ENSP00000225964.5:p.Val1057Gly
|
|
ENST00000511732.1:n.114T>G
|
|
|
NM_000088.3:c.3170T>G , LRG_1t1:c.3170T>G
|
NP_000079.2:p.Val1057Gly
|
|
XM_005257058.3:c.2900T>G
|
XP_005257115.2:p.Val967Gly
|
|
XM_005257059.3:c.2252T>G
|
XP_005257116.2:p.Val751Gly
|
|
XM_011524341.1:c.2972T>G
|
XP_011522643.1:p.Val991Gly
|
|
XM_005257058.4:c.2900T>G
|
XP_005257115.2:p.Val967Gly
|
|
XM_005257059.4:c.2252T>G
|
XP_005257116.2:p.Val751Gly
|
|
NM_000088.4:c.3170T>G
MANE Select
|
NP_000079.2:p.Val1057Gly
|
|