ENST00000555134.2:n.1002G>T
|
|
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ENST00000556394.2:c.1618G>T
|
ENSP00000451967.2:p.Ala540Ser
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ENST00000682247.1:c.2066G>T
|
ENSP00000507213.1:p.Gly689Val
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ENST00000682395.1:n.2541G>T
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ENST00000682459.1:n.1780G>T
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ENST00000682467.1:c.1936G>T
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ENSP00000508062.1:p.Ala646Ser
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ENST00000682795.1:c.2224G>T
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ENSP00000507574.1:p.Ala742Ser
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ENST00000682895.1:n.1793G>T
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ENST00000682955.1:n.1651G>T
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ENST00000683188.1:c.2338G>T
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ENST00000683380.1:n.1741G>T
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|
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ENST00000683907.1:c.342G>T
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ENSP00000507754.1:n.342G>T
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ENST00000684259.1:n.3844G>T
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ENST00000684538.1:n.1456G>T
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ENST00000684549.1:n.1628G>T
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ENST00000261534.9:c.2077G>T
MANE Select
|
ENSP00000261534.4:p.Ala693Ser
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ENST00000261534.8:c.2077G>T
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ENSP00000261534.4:p.Ala693Ser
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ENST00000452340.7:n.3053G>T
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|
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ENST00000554767.5:n.2863G>T
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|
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ENST00000555710.1:c.438G>T
|
ENSP00000451730.1:n.438G>T
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ENST00000556394.1:c.132G>T
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|
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ENST00000556446.1:n.378G>T
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ENST00000602717.5:c.292G>T
|
ENSP00000487704.1:p.Ala98Ser
|
|
NM_013382.5:c.2077G>T , LRG_844t1:c.2077G>T
|
NP_037514.2:p.Ala693Ser
|
|
XM_011536675.1:c.2266G>T
|
XP_011534977.1:p.Ala756Ser
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|
XM_011536676.1:c.1933G>T
|
XP_011534978.1:p.Ala645Ser
|
|
XM_011536677.1:c.1807G>T
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XP_011534979.1:p.Ala603Ser
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|
XM_011536679.1:c.1360G>T
|
XP_011534981.1:p.Ala454Ser
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XR_943416.1:n.2330G>T
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|
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XM_011536675.2:c.2266G>T
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XP_011534977.1:p.Ala756Ser
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|
XM_011536676.2:c.1933G>T
|
XP_011534978.1:p.Ala645Ser
|
|
XM_011536677.3:c.1807G>T
|
XP_011534979.1:p.Ala603Ser
|
|
XR_001750279.1:n.2363G>T
|
|
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XR_001750282.1:n.3016G>T
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XR_943416.3:n.2328G>T
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NM_013382.6:c.2077G>T
|
NP_037514.2:p.Ala693Ser
|
|
NM_013382.7:c.2077G>T
MANE Select
|
NP_037514.2:p.Ala693Ser
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