ENST00000622290.5:c.2966G>T
|
ENSP00000483331.2:p.Gly989Val
|
|
ENST00000205557.12:c.2966G>T
MANE Select
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ENSP00000205557.7:p.Gly989Val
|
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ENST00000205557.11:c.2966G>T
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ENSP00000205557.7:p.Gly989Val
|
|
ENST00000456970.6:c.2791G>T
|
ENSP00000405002.2:n.2791G>T
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ENST00000622290.4:c.*175G>T
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ENSP00000483331.1:n.*175G>T
|
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NM_001171.5:c.2966G>T
|
NP_001162.4:p.Gly989Val
|
|
XM_011522479.1:c.2933G>T
|
XP_011520781.1:p.Gly978Val
|
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XM_011522480.1:c.2624G>T
|
XP_011520782.1:p.Gly875Val
|
|
XM_011522481.1:c.2624G>T
|
XP_011520783.1:p.Gly875Val
|
|
XR_932836.1:n.3201G>T
|
|
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XR_932837.1:n.3202G>T
|
|
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XR_932838.1:n.3202G>T
|
|
|
NM_001351800.1:c.2624G>T
|
NP_001338729.1:p.Gly875Val
|
|
NR_147784.1:n.2828G>T
|
|
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XM_011522479.2:c.2933G>T
|
XP_011520781.1:p.Gly978Val
|
|
XM_011522481.3:c.2624G>T
|
XP_011520783.1:p.Gly875Val
|
|
XM_017023212.1:c.2798G>T
|
XP_016878701.1:p.Gly933Val
|
|
XM_017023214.1:c.2966G>T
|
XP_016878703.1:p.Gly989Val
|
|
XM_024450261.1:c.3002G>T
|
XP_024306029.1:p.Gly1001Val
|
|
XR_932836.2:n.3147G>T
|
|
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XR_932837.3:n.3147G>T
|
|
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XR_932838.3:n.3147G>T
|
|
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NM_001171.6:c.2966G>T
MANE Select
|
NP_001162.5:p.Gly989Val
|
|