ENST00000649276.2:c.1489G>A
MANE Select
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ENSP00000497003.1:p.Gly497Ser
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ENST00000329705.11:c.1009+839G>A
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ENSP00000331176.7:n.1009+839G>A
|
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ENST00000332710.8:c.1462G>A
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ENSP00000331791.4:p.Gly488Ser
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ENST00000359500.7:c.1009+839G>A
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ENSP00000352483.3:n.1009+839G>A
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ENST00000621939.1:c.1009+839G>A
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ENSP00000477982.1:n.1009+839G>A
|
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NM_005992.1:c.1009+839G>A
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NP_005983.1:n.1009+839G>A
|
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NM_080646.1:c.1009+839G>A
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NP_542377.1:n.1009+839G>A
|
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NM_080647.1:c.1462G>A , LRG_226t1:c.1462G>A
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NP_542378.1:p.Gly488Ser
|
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XM_006724312.1:c.1462G>A
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XP_006724375.1:p.Gly488Ser
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|
XM_011530351.1:c.1489G>A
|
XP_011528653.1:p.Gly497Ser
|
|
XM_006724312.2:c.1462G>A
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XP_006724375.1:p.Gly488Ser
|
|
XM_017028925.1:c.1612G>A
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XP_016884414.1:p.Gly538Ser
|
|
XM_017028926.1:c.1462G>A
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XP_016884415.1:p.Gly488Ser
|
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XM_017028927.1:c.817G>A
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XP_016884416.1:p.Gly273Ser
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|
XM_017028928.1:c.1159+839G>A
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XP_016884417.1:n.1159+839G>A
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NM_001379200.1:c.1489G>A
MANE Select
|
NP_001366129.1:p.Gly497Ser
|
|
NM_080646.2:c.1009+839G>A
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NP_542377.1:n.1009+839G>A
|
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