ENST00000378585.7:c.85G>A
MANE Select
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ENSP00000367848.4:p.Gly29Ser
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ENST00000638411.1:c.85G>A
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ENSP00000491632.1:p.Gly29Ser
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ENST00000638604.1:n.149G>A
|
|
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ENST00000638771.1:c.85G>A
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ENSP00000492435.1:p.Gly29Ser
|
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ENST00000639045.1:c.*71G>A
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ENSP00000491997.1:n.*71G>A
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ENST00000639777.1:n.689G>A
|
|
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ENST00000639935.1:n.122G>A
|
|
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ENST00000640030.1:c.25G>A
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ENSP00000491411.1:p.Gly9Ser
|
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ENST00000640067.1:c.85G>A
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ENSP00000491844.1:p.Gly29Ser
|
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ENST00000640423.1:n.94G>A
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|
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ENST00000640949.1:c.85G>A
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ENSP00000492500.1:p.Gly29Ser
|
|
ENST00000378585.5:c.85G>A
|
ENSP00000367848.4:p.Gly29Ser
|
|
NM_000815.4:c.85G>A
|
NP_000806.2:p.Gly29Ser
|
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XM_011541194.1:c.124G>A
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XP_011539496.1:p.Gly42Ser
|
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XM_011541194.3:c.124G>A
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XP_011539496.1:p.Gly42Ser
|
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XM_017000936.1:c.790G>A
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XP_016856425.1:p.Gly264Ser
|
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NM_000815.5:c.85G>A
MANE Select
|
NP_000806.2:p.Gly29Ser
|
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