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NM_000088.4:c.3871T>G
MANE Select
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NP_000079.2:p.Cys1291Gly
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|
ENST00000225964.10:c.3871T>G
MANE Select
|
ENSP00000225964.6:p.Cys1291Gly
|
|
NM_000088.3:c.3871T>G , LRG_1t1:c.3871T>G
|
NP_000079.2:p.Cys1291Gly
|
|
ENST00000225964.9:c.3871T>G
|
ENSP00000225964.5:p.Cys1291Gly
|
|
ENST00000510710.3:n.540T>G
|
|
|
XM_005257058.3:c.3601T>G
|
XP_005257115.2:p.Cys1201Gly
|
|
XM_005257058.4:c.3601T>G
|
XP_005257115.2:p.Cys1201Gly
|
|
XM_005257059.3:c.2953T>G
|
XP_005257116.2:p.Cys985Gly
|
|
XM_005257059.4:c.2953T>G
|
XP_005257116.2:p.Cys985Gly
|
|
XM_011524341.1:c.3673T>G
|
XP_011522643.1:p.Cys1225Gly
|