ENST00000262304.9:c.5451G=
MANE Select
|
ENSP00000262304.4:p.Val1817=
|
|
ENST00000262304.8:c.5451G=
|
ENSP00000262304.4:p.Val1817=
|
|
ENST00000415938.7:n.310+2624G=
|
|
|
ENST00000423118.5:c.5451G=
|
ENSP00000399501.1:p.Val1817=
|
|
ENST00000468674.5:n.431-366G=
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|
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ENST00000483024.1:c.233+2100G=
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|
|
ENST00000483731.5:n.790+2624G=
|
|
|
ENST00000487932.5:c.138G=
|
ENSP00000457132.1:p.Val46=
|
|
ENST00000488185.2:c.473-1358G=
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|
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ENST00000565639.6:n.773+2624G=
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|
|
ENST00000568591.5:c.2226+2624G=
|
ENSP00000457162.1:n.2226+2624G=
|
|
ENST00000569983.5:n.421+2624G=
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|
|
NM_000296.3:c.5451G=
|
NP_000287.3:p.Val1817=
|
|
NM_001009944.2:c.5451G=
|
NP_001009944.2:p.Val1817=
|
|
XM_005255370.2:c.2406G=
|
XP_005255427.1:p.Val802=
|
|
XM_011522525.1:c.5529G=
|
XP_011520827.1:p.Val1843=
|
|
XM_011522526.1:c.5529G=
|
XP_011520828.1:p.Val1843=
|
|
XM_011522527.1:c.5529G=
|
XP_011520829.1:p.Val1843=
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|
XM_011522528.1:c.5505G=
|
XP_011520830.1:p.Val1835=
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|
XM_011522529.1:c.5505G=
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XP_011520831.1:p.Val1835=
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|
XM_011522530.1:c.5475G=
|
XP_011520832.1:p.Val1825=
|
|
XM_011522531.1:c.5457G=
|
XP_011520833.1:p.Val1819=
|
|
XM_011522532.1:c.5403G=
|
XP_011520834.1:p.Val1801=
|
|
XM_011522533.1:c.5322G=
|
XP_011520835.1:p.Val1774=
|
|
XM_011522534.1:c.5265G=
|
XP_011520836.1:p.Val1755=
|
|
XM_011522535.1:c.3351G=
|
XP_011520837.1:p.Val1117=
|
|
XM_011522536.1:c.5529G=
|
XP_011520838.1:p.Val1843=
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|
XM_011522537.1:c.2529G=
|
XP_011520839.1:p.Val843=
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|
XR_932867.1:n.5544G=
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XR_932868.1:n.5544G=
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|
XR_932869.1:n.5544G=
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|
|
XR_932870.1:n.5544G=
|
|
|
XM_005255370.3:c.2406G=
|
XP_005255427.1:p.Val802=
|
|
XM_011522528.3:c.5505G=
|
XP_011520830.1:p.Val1835=
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|
XM_011522529.2:c.5505G=
|
XP_011520831.1:p.Val1835=
|
|
XM_011522537.2:c.2529G=
|
XP_011520839.1:p.Val843=
|
|
XM_024450298.1:c.5571G=
|
XP_024306066.1:p.Val1857=
|
|
XM_024450299.1:c.5499G=
|
XP_024306067.1:p.Val1833=
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|
XM_024450300.1:c.5361G=
|
XP_024306068.1:p.Val1787=
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|
XM_024450301.1:c.3447G=
|
XP_024306069.1:p.Val1149=
|
|
NM_000296.4:c.5451G=
|
NP_000287.4:p.Val1817=
|
|
NM_001009944.3:c.5451G=
MANE Select
|
NP_001009944.3:p.Val1817=
|
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