ENST00000324662.8:c.1223G>T
|
ENSP00000313419.4:p.Gly408Val
|
|
ENST00000538922.8:c.1223G>T
MANE Select
|
ENSP00000437940.2:p.Gly408Val
|
|
ENST00000324662.7:c.1223G>T
|
ENSP00000313419.3:p.Gly408Val
|
|
ENST00000538922.5:c.1223G>T
|
ENSP00000437940.1:p.Gly408Val
|
|
ENST00000565089.5:n.1557G>T
|
|
|
ENST00000567368.1:n.363G>T
|
|
|
ENST00000567541.5:c.1223G>T
|
ENSP00000456201.1:p.Gly408Val
|
|
ENST00000611258.4:c.1222G>T
|
ENSP00000481090.1:p.Ala408Ser
|
|
NM_001178098.1:c.1223G>T
|
NP_001171569.1:p.Gly408Val
|
|
NM_001770.5:c.1223G>T , LRG_35t1:c.1223G>T
|
NP_001761.3:p.Gly408Val
|
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XM_006721103.2:c.956G>T
|
XP_006721166.1:p.Gly319Val
|
|
XM_006721103.3:c.956G>T
|
XP_006721166.1:p.Gly319Val
|
|
XM_017023893.1:c.956G>T
|
XP_016879382.1:p.Gly319Val
|
|
NM_001178098.2:c.1223G>T
|
NP_001171569.1:p.Gly408Val
|
|
NM_001770.6:c.1223G>T
MANE Select
|
NP_001761.3:p.Gly408Val
|
|
NM_001385732.1:c.956G>T
|
NP_001372661.1:p.Gly319Val
|
|
NR_169755.1:n.1565G>T
|
|
|