ENST00000339077.10:c.947G>C
MANE Select
|
ENSP00000343273.4:p.Trp316Ser
|
|
ENST00000339077.9:c.947G>C
|
ENSP00000343273.4:p.Trp316Ser
|
|
ENST00000409689.5:c.803G>C
|
ENSP00000386263.1:p.Trp268Ser
|
|
ENST00000521082.5:c.*955G>C
|
ENSP00000430351.1:n.*955G>C
|
|
NM_001031710.2:c.947G>C
|
NP_001026880.2:p.Trp316Ser
|
|
NM_018846.4:c.803G>C
|
NP_061334.4:p.Trp268Ser
|
|
NR_033328.1:n.1371G>C
|
|
|
XM_006715753.1:c.986G>C
|
XP_006715816.1:p.Trp329Ser
|
|
XM_006715754.1:c.920G>C
|
XP_006715817.1:p.Trp307Ser
|
|
XM_006715755.1:c.920G>C
|
XP_006715818.1:p.Trp307Ser
|
|
XM_006715756.1:c.842G>C
|
XP_006715819.1:p.Trp281Ser
|
|
XM_006715753.3:c.986G>C
|
XP_006715816.1:p.Trp329Ser
|
|
XM_006715754.3:c.920G>C
|
XP_006715817.1:p.Trp307Ser
|
|
XM_006715755.3:c.920G>C
|
XP_006715818.1:p.Trp307Ser
|
|
XM_006715756.3:c.842G>C
|
XP_006715819.1:p.Trp281Ser
|
|
XM_017012439.2:c.881G>C
|
XP_016867928.1:p.Trp294Ser
|
|
NM_001031710.3:c.947G>C
MANE Select
|
NP_001026880.2:p.Trp316Ser
|
|
NM_018846.5:c.803G>C
|
NP_061334.4:p.Trp268Ser
|
|
NR_033328.2:n.1320G>C
|
|
|