ENST00000225964.10:c.1727A>G
MANE Select
|
ENSP00000225964.6:p.Gln576Arg
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|
ENST00000225964.9:c.1727A>G
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ENSP00000225964.5:p.Gln576Arg
|
|
ENST00000463440.1:n.117A>G
|
|
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ENST00000471344.1:n.759A>G
|
|
|
ENST00000476387.1:n.76A>G
|
|
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NM_000088.3:c.1727A>G , LRG_1t1:c.1727A>G
|
NP_000079.2:p.Gln576Arg
|
|
XM_005257058.3:c.1727A>G
|
XP_005257115.2:p.Gln576Arg
|
|
XM_005257059.3:c.958-1290A>G
|
XP_005257116.2:n.958-1290A>G
|
|
XM_011524341.1:c.1529A>G
|
XP_011522643.1:p.Gln510Arg
|
|
XM_005257058.4:c.1727A>G
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XP_005257115.2:p.Gln576Arg
|
|
XM_005257059.4:c.958-1290A>G
|
XP_005257116.2:n.958-1290A>G
|
|
NM_000088.4:c.1727A>G
MANE Select
|
NP_000079.2:p.Gln576Arg
|
|