ENST00000372563.2:c.955A>G
MANE Select
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ENSP00000361644.1:p.Thr319Ala
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ENST00000327674.8:c.955A>G
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ENSP00000329374.4:p.Thr319Ala
|
|
ENST00000372563.1:c.955A>G
|
ENSP00000361644.1:p.Thr319Ala
|
|
ENST00000487487.1:n.228A>G
|
|
|
NM_000354.5:c.955A>G
|
NP_000345.2:p.Thr319Ala
|
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XM_005262180.3:c.955A>G
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XP_005262237.1:p.Thr319Ala
|
|
XM_006724683.1:c.955A>G
|
XP_006724746.1:p.Thr319Ala
|
|
XM_005262180.4:c.955A>G
|
XP_005262237.1:p.Thr319Ala
|
|
XM_006724683.2:c.955A>G
|
XP_006724746.1:p.Thr319Ala
|
|
NM_000354.6:c.955A>G
MANE Select
|
NP_000345.2:p.Thr319Ala
|
|