ENST00000710323.1:c.673G>A
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ENSP00000518203.1:p.Ala225Thr
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|
ENST00000330877.7:c.673G>A
MANE Select
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ENSP00000331260.2:p.Ala225Thr
|
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ENST00000330877.6:c.673G>A
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ENSP00000331260.2:p.Ala225Thr
|
|
ENST00000332972.9:c.802G>A
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ENSP00000333019.5:p.Ala268Thr
|
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ENST00000553540.5:c.785G>A
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ENSP00000450759.1:n.785G>A
|
|
ENST00000555486.5:c.738G>A
|
ENSP00000473778.1:n.738G>A
|
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ENST00000557582.5:n.1594G>A
|
|
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NM_152328.3:c.673G>A
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NP_689541.1:p.Ala225Thr
|
|
NM_199165.1:c.802G>A
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NP_954634.1:p.Ala268Thr
|
|
XM_006720026.2:c.676G>A
|
XP_006720089.1:p.Ala226Thr
|
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XM_011536412.1:c.805G>A
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XP_011534714.1:p.Ala269Thr
|
|
XM_011536413.1:c.490G>A
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XP_011534715.1:p.Ala164Thr
|
|
XM_011536414.1:c.487G>A
|
XP_011534716.1:p.Ala163Thr
|
|
XM_011536415.1:c.58G>A
|
XP_011534717.1:p.Ala20Thr
|
|
NM_001320424.1:c.58G>A
|
NP_001307353.1:p.Ala20Thr
|
|
NM_152328.4:c.673G>A
|
NP_689541.1:p.Ala225Thr
|
|
NM_199165.2:c.802G>A
|
NP_954634.1:p.Ala268Thr
|
|
XM_006720026.3:c.676G>A
|
XP_006720089.1:p.Ala226Thr
|
|
XM_011536412.2:c.805G>A
|
XP_011534714.1:p.Ala269Thr
|
|
NM_152328.5:c.673G>A
MANE Select
|
NP_689541.1:p.Ala225Thr
|
|