ENST00000357103.5:c.582C>G
MANE Select
|
ENSP00000349616.4:p.Cys194Trp
|
|
ENST00000357103.4:c.582C>G
|
ENSP00000349616.4:p.Cys194Trp
|
|
ENST00000537190.1:n.422C>G
|
|
|
NM_024551.2:c.582C>G
|
NP_078827.2:p.Cys194Trp
|
|
XM_005253789.1:c.582C>G
|
XP_005253846.1:p.Cys194Trp
|
|
XM_006719018.1:c.582C>G
|
XP_006719081.1:p.Cys194Trp
|
|
XM_011521024.1:c.582C>G
|
XP_011519326.1:p.Cys194Trp
|
|
XM_011521025.1:c.463+2544C>G
|
XP_011519327.1:n.463+2544C>G
|
|
XM_005253789.2:c.582C>G
|
XP_005253846.1:p.Cys194Trp
|
|
XM_006719018.2:c.582C>G
|
XP_006719081.1:p.Cys194Trp
|
|
XM_011521024.2:c.582C>G
|
XP_011519326.1:p.Cys194Trp
|
|
NM_024551.3:c.582C>G
MANE Select
|
NP_078827.2:p.Cys194Trp
|
|
NM_001375363.1:c.582C>G
|
NP_001362292.1:p.Cys194Trp
|
|
NM_001375364.1:c.582C>G
|
NP_001362293.1:p.Cys194Trp
|
|
NM_001375365.1:c.582C>G
|
NP_001362294.1:p.Cys194Trp
|
|