ENST00000336840.11:c.775A>G
|
ENSP00000338767.5:p.Thr259Ala
|
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ENST00000344493.9:c.775A>G
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ENSP00000342092.4:p.Thr259Ala
|
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ENST00000350526.9:c.775A>G
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ENSP00000343052.4:p.Thr259Ala
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ENST00000392070.7:c.775A>G
MANE Select
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ENSP00000375922.3:p.Thr259Ala
|
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ENST00000646154.1:n.589A>G
|
|
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ENST00000336840.10:c.775A>G
|
ENSP00000338767.5:p.Thr259Ala
|
|
ENST00000344493.8:c.775A>G
|
ENSP00000342092.4:p.Thr259Ala
|
|
ENST00000350526.8:c.775A>G
|
ENSP00000343052.4:p.Thr259Ala
|
|
ENST00000392069.6:c.775A>G
|
ENSP00000375921.2:p.Thr259Ala
|
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ENST00000392070.6:c.775A>G
|
ENSP00000375922.2:p.Thr259Ala
|
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ENST00000409551.7:c.772A>G
|
ENSP00000386750.3:p.Thr258Ala
|
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NM_001127366.2:c.772A>G
|
NP_001120838.1:p.Thr258Ala
|
|
NM_181457.3:c.775A>G
|
NP_852122.1:p.Thr259Ala
|
|
NM_181458.3:c.775A>G
|
NP_852123.1:p.Thr259Ala
|
|
NM_181459.3:c.775A>G
|
NP_852124.1:p.Thr259Ala
|
|
NM_181460.3:c.775A>G
|
NP_852125.1:p.Thr259Ala
|
|
NM_181461.3:c.775A>G
|
NP_852126.1:p.Thr259Ala
|
|
XM_011511278.1:c.919A>G
|
XP_011509580.1:p.Thr307Ala
|
|
XM_011511279.1:c.211A>G
|
XP_011509581.1:p.Thr71Ala
|
|
XR_923945.1:n.287+10125T>C
|
|
|
NM_001127366.3:c.772A>G
|
NP_001120838.1:p.Thr258Ala
|
|
NM_181457.4:c.775A>G
|
NP_852122.1:p.Thr259Ala
|
|
NM_181458.4:c.775A>G
MANE Select
|
NP_852123.1:p.Thr259Ala
|
|
NM_181459.4:c.775A>G
|
NP_852124.1:p.Thr259Ala
|
|
NM_181460.4:c.775A>G
|
NP_852125.1:p.Thr259Ala
|
|
NM_181461.4:c.775A>G
|
NP_852126.1:p.Thr259Ala
|
|