ENST00000382099.3:c.984G>T
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ENST00000382100.8:c.1426G>T
MANE Select
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ENSP00000371532.2:p.Ala476Ser
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ENST00000478776.2:n.871G>T
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ENST00000679718.1:n.662G>T
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|
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ENST00000679750.1:n.842G>T
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ENST00000679851.1:n.1610G>T
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ENST00000680021.1:n.1626G>T
|
|
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ENST00000680043.1:c.978G>T
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|
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ENST00000680219.1:c.993G>T
|
|
|
ENST00000680243.1:c.*1205G>T
|
ENSP00000505911.1:n.*1205G>T
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ENST00000680296.1:c.852G>T
|
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ENST00000680332.1:n.509G>T
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ENST00000680746.1:c.1303G>T
|
ENSP00000505030.1:p.Ala435Ser
|
|
ENST00000680751.1:n.831G>T
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|
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ENST00000680891.1:c.*1218G>T
|
ENSP00000505167.1:n.*1218G>T
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ENST00000680975.1:n.811G>T
|
|
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ENST00000681087.1:n.871G>T
|
|
|
ENST00000681306.1:c.1426G>T
|
ENSP00000506072.1:p.Ala476Ser
|
|
ENST00000681618.1:c.1303G>T
|
ENSP00000505773.1:p.Ala435Ser
|
|
ENST00000681644.1:c.*1098G>T
|
ENSP00000505180.1:n.*1098G>T
|
|
ENST00000681806.1:c.1426G>T
|
ENSP00000505282.1:p.Ala476Ser
|
|
ENST00000681942.1:c.974G>T
|
|
|
ENST00000382099.2:c.1426G>T
|
ENSP00000371531.2:p.Ala476Ser
|
|
ENST00000382100.7:c.1426G>T
|
ENSP00000371532.2:p.Ala476Ser
|
|
NM_001018056.1:c.1426G>T
|
NP_001018066.1:p.Ala476Ser
|
|
NM_003383.3:c.1426G>T
|
NP_003374.3:p.Ala476Ser
|
|
XM_011518029.1:c.1303G>T
|
XP_011516331.1:p.Ala435Ser
|
|
NM_001018056.2:c.1426G>T
|
NP_001018066.1:p.Ala476Ser
|
|
NM_001322225.1:c.1303G>T
|
NP_001309154.1:p.Ala435Ser
|
|
NM_001322226.1:c.1303G>T
|
NP_001309155.1:p.Ala435Ser
|
|
NM_003383.4:c.1426G>T
|
NP_003374.3:p.Ala476Ser
|
|
XR_001746373.2:n.1830G>T
|
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XR_002956805.1:n.1830G>T
|
|
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NM_003383.5:c.1426G>T
MANE Select
|
NP_003374.3:p.Ala476Ser
|
|
NM_001018056.3:c.1426G>T
|
NP_001018066.1:p.Ala476Ser
|
|
NM_001322225.2:c.1303G>T
|
NP_001309154.1:p.Ala435Ser
|
|
NM_001322226.2:c.1303G>T
|
NP_001309155.1:p.Ala435Ser
|
|