ENST00000262304.9:c.7234A>G
MANE Select
|
ENSP00000262304.4:p.Asn2412Asp
|
|
ENST00000262304.8:c.7234A>G
|
ENSP00000262304.4:p.Asn2412Asp
|
|
ENST00000415938.7:n.479A>G
|
|
|
ENST00000423118.5:c.7234A>G
|
ENSP00000399501.1:p.Asn2412Asp
|
|
ENST00000483024.1:c.402A>G
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|
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ENST00000483558.5:n.293A>G
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|
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ENST00000483731.5:n.959A>G
|
|
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ENST00000486339.6:n.980A>G
|
|
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ENST00000487932.5:c.1921A>G
|
ENSP00000457132.1:p.Asn641Asp
|
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ENST00000496574.6:n.1237A>G
|
|
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ENST00000565639.6:n.942A>G
|
|
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ENST00000568591.5:c.2395A>G
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ENSP00000457162.1:n.2395A>G
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|
ENST00000569983.5:n.590A>G
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|
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NM_000296.3:c.7234A>G
|
NP_000287.3:p.Asn2412Asp
|
|
NM_001009944.2:c.7234A>G
|
NP_001009944.2:p.Asn2412Asp
|
|
XM_005255370.2:c.4189A>G
|
XP_005255427.1:p.Asn1397Asp
|
|
XM_011522525.1:c.7312A>G
|
XP_011520827.1:p.Asn2438Asp
|
|
XM_011522526.1:c.7312A>G
|
XP_011520828.1:p.Asn2438Asp
|
|
XM_011522527.1:c.7312A>G
|
XP_011520829.1:p.Asn2438Asp
|
|
XM_011522528.1:c.7288A>G
|
XP_011520830.1:p.Asn2430Asp
|
|
XM_011522529.1:c.7288A>G
|
XP_011520831.1:p.Asn2430Asp
|
|
XM_011522530.1:c.7258A>G
|
XP_011520832.1:p.Asn2420Asp
|
|
XM_011522531.1:c.7240A>G
|
XP_011520833.1:p.Asn2414Asp
|
|
XM_011522532.1:c.7186A>G
|
XP_011520834.1:p.Asn2396Asp
|
|
XM_011522533.1:c.7105A>G
|
XP_011520835.1:p.Asn2369Asp
|
|
XM_011522534.1:c.7048A>G
|
XP_011520836.1:p.Asn2350Asp
|
|
XM_011522535.1:c.5134A>G
|
XP_011520837.1:p.Asn1712Asp
|
|
XM_011522536.1:c.7312A>G
|
XP_011520838.1:p.Asn2438Asp
|
|
XM_011522537.1:c.4312A>G
|
XP_011520839.1:p.Asn1438Asp
|
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XR_932867.1:n.7327A>G
|
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XR_932868.1:n.7327A>G
|
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XR_932869.1:n.7327A>G
|
|
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XR_932870.1:n.7327A>G
|
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XM_005255370.3:c.4189A>G
|
XP_005255427.1:p.Asn1397Asp
|
|
XM_011522528.3:c.7288A>G
|
XP_011520830.1:p.Asn2430Asp
|
|
XM_011522529.2:c.7288A>G
|
XP_011520831.1:p.Asn2430Asp
|
|
XM_011522537.2:c.4312A>G
|
XP_011520839.1:p.Asn1438Asp
|
|
XM_024450298.1:c.7354A>G
|
XP_024306066.1:p.Asn2452Asp
|
|
XM_024450299.1:c.7282A>G
|
XP_024306067.1:p.Asn2428Asp
|
|
XM_024450300.1:c.7144A>G
|
XP_024306068.1:p.Asn2382Asp
|
|
XM_024450301.1:c.5230A>G
|
XP_024306069.1:p.Asn1744Asp
|
|
NM_000296.4:c.7234A>G
|
NP_000287.4:p.Asn2412Asp
|
|
NM_001009944.3:c.7234A>G
MANE Select
|
NP_001009944.3:p.Asn2412Asp
|
|