ENST00000335757.10:c.467G>T
MANE Select
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ENSP00000336888.4:p.Gly156Val
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ENST00000335757.9:c.467G>T
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ENSP00000336888.4:p.Gly156Val
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ENST00000407327.8:c.461G>T
|
ENSP00000385135.3:p.Gly154Val
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ENST00000586078.5:c.467G>T
|
ENSP00000466664.1:p.Gly156Val
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ENST00000588409.1:c.246-3256G>T
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ENSP00000468070.1:n.246-3256G>T
|
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ENST00000588465.5:n.376G>T
|
|
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ENST00000588688.5:c.308G>T
|
ENSP00000467552.1:p.Gly103Val
|
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ENST00000590382.5:c.302G>T
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ENSP00000468691.1:p.Gly101Val
|
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ENST00000590857.5:c.-83G>T
|
ENSP00000465547.1:n.-83G>T
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ENST00000592293.5:c.*264G>T
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ENSP00000466612.1:n.*264G>T
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|
NM_001145056.1:c.461G>T
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NP_001138528.1:p.Gly154Val
|
|
NM_020428.3:c.467G>T
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NP_065161.3:p.Gly156Val
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|
XM_005259997.1:c.467G>T
|
XP_005260054.1:p.Gly156Val
|
|
XM_005259999.1:c.461G>T
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XP_005260056.1:p.Gly154Val
|
|
NM_001363611.1:c.467G>T
|
NP_001350540.1:p.Gly156Val
|
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XM_005259999.2:c.461G>T
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XP_005260056.1:p.Gly154Val
|
|
NM_020428.4:c.467G>T
MANE Select
|
NP_065161.3:p.Gly156Val
|
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NM_001145056.2:c.461G>T
|
NP_001138528.1:p.Gly154Val
|
|
NM_001363611.2:c.467G>T
|
NP_001350540.1:p.Gly156Val
|
|