ENST00000339077.10:c.1134T>G
MANE Select
|
ENSP00000343273.4:p.Cys378Trp
|
|
ENST00000339077.9:c.1134T>G
|
ENSP00000343273.4:p.Cys378Trp
|
|
ENST00000409689.5:c.990T>G
|
ENSP00000386263.1:p.Cys330Trp
|
|
ENST00000469576.1:n.21T>G
|
|
|
ENST00000521082.5:c.*1142T>G
|
ENSP00000430351.1:n.*1142T>G
|
|
NM_001031710.2:c.1134T>G
|
NP_001026880.2:p.Cys378Trp
|
|
NM_018846.4:c.990T>G
|
NP_061334.4:p.Cys330Trp
|
|
NR_033328.1:n.1558T>G
|
|
|
XM_006715753.1:c.1173T>G
|
XP_006715816.1:p.Cys391Trp
|
|
XM_006715754.1:c.1107T>G
|
XP_006715817.1:p.Cys369Trp
|
|
XM_006715755.1:c.1107T>G
|
XP_006715818.1:p.Cys369Trp
|
|
XM_006715756.1:c.1029T>G
|
XP_006715819.1:p.Cys343Trp
|
|
XM_006715753.3:c.1173T>G
|
XP_006715816.1:p.Cys391Trp
|
|
XM_006715754.3:c.1107T>G
|
XP_006715817.1:p.Cys369Trp
|
|
XM_006715755.3:c.1107T>G
|
XP_006715818.1:p.Cys369Trp
|
|
XM_006715756.3:c.1029T>G
|
XP_006715819.1:p.Cys343Trp
|
|
XM_017012439.2:c.1068T>G
|
XP_016867928.1:p.Cys356Trp
|
|
NM_001031710.3:c.1134T>G
MANE Select
|
NP_001026880.2:p.Cys378Trp
|
|
NM_018846.5:c.990T>G
|
NP_061334.4:p.Cys330Trp
|
|
NR_033328.2:n.1507T>G
|
|
|