ENST00000347401.8:c.941G>T
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ENST00000353578.9:c.7678G>T
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ENSP00000315873.4:p.Gly2560Cys
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ENST00000682957.1:c.299G>T
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ENST00000684508.1:n.563G>T
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ENST00000295550.9:c.8296G>T
MANE Select
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ENSP00000295550.4:p.Gly2766Cys
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ENST00000295550.8:c.8296G>T
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ENSP00000295550.4:p.Gly2766Cys
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ENST00000347401.7:c.6472G>T
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ENSP00000315609.4:p.Gly2158Cys
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ENST00000353578.8:c.7678G>T
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ENSP00000315873.4:p.Gly2560Cys
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ENST00000409809.5:c.7678G>T
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ENSP00000386844.1:p.Gly2560Cys
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ENST00000472056.5:c.6475G>T
|
ENSP00000418285.1:p.Gly2159Cys
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ENST00000491769.1:n.4738G>T
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NM_004369.3:c.8296G>T , LRG_473t1:c.8296G>T
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NP_004360.2:p.Gly2766Cys
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NM_057166.4:c.6475G>T
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NP_476507.3:p.Gly2159Cys
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NM_057167.3:c.7678G>T
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NP_476508.2:p.Gly2560Cys
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|
XM_005246065.1:c.7696G>T
|
XP_005246122.1:p.Gly2566Cys
|
|
XM_005246066.1:c.7075G>T
|
XP_005246123.1:p.Gly2359Cys
|
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XM_006712253.1:c.7795G>T
|
XP_006712316.1:p.Gly2599Cys
|
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XM_011510574.1:c.8293G>T
|
XP_011508876.1:p.Gly2765Cys
|
|
XM_011510575.1:c.5890G>T
|
XP_011508877.1:p.Gly1964Cys
|
|
XM_017003304.1:c.5890G>T
|
XP_016858793.1:p.Gly1964Cys
|
|
XM_024452684.1:c.7075G>T
|
XP_024308452.1:p.Gly2359Cys
|
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NM_004369.4:c.8296G>T
MANE Select
|
NP_004360.2:p.Gly2766Cys
|
|
NM_057166.5:c.6475G>T
|
NP_476507.3:p.Gly2159Cys
|
|
NM_057167.4:c.7678G>T
|
NP_476508.2:p.Gly2560Cys
|
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