|
NM_001790.5:c.1351A>G
MANE Select
|
NP_001781.2:p.Ser451Gly
|
|
ENST00000323760.11:c.1351A>G
MANE Select
|
ENSP00000321656.6:p.Ser451Gly
|
|
NM_001287582.1:c.1351A>G
|
NP_001274511.1:p.Ser451Gly
|
|
NM_001287582.2:c.1351A>G
|
NP_001274511.1:p.Ser451Gly
|
|
NM_001287583.1:c.1585A>G
|
NP_001274512.1:p.Ser529Gly
|
|
NM_001287583.2:c.1585A>G
|
NP_001274512.1:p.Ser529Gly
|
|
NM_001318098.1:c.1402A>G
|
NP_001305027.1:p.Ser468Gly
|
|
NM_001318098.2:c.1402A>G
|
NP_001305027.1:p.Ser468Gly
|
|
NM_001364026.1:c.1522A>G
|
NP_001350955.1:p.Ser508Gly
|
|
NM_001364027.1:c.1249A>G
|
NP_001350956.1:p.Ser417Gly
|
|
NM_001364028.1:c.1222A>G
|
NP_001350957.1:p.Ser408Gly
|
|
NM_001790.4:c.1351A>G
|
NP_001781.2:p.Ser451Gly
|
|
NM_022809.3:c.1132A>G
|
NP_073720.1:p.Ser378Gly
|
|
NM_022809.4:c.1132A>G
|
NP_073720.1:p.Ser378Gly
|
|
ENST00000323760.10:c.1351A>G
|
ENSP00000321656.6:p.Ser451Gly
|
|
ENST00000348983.7:c.1132A>G
|
ENSP00000345205.3:p.Ser378Gly
|
|
ENST00000415130.6:c.1132A>G
|
ENSP00000392631.2:p.Ser378Gly
|
|
ENST00000513970.5:c.1351A>G
|
ENSP00000424795.1:p.Ser451Gly
|
|
ENST00000514017.1:c.755A>G
|
|
|
ENST00000514555.5:c.1261A>G
|
ENSP00000425470.1:p.Ser421Gly
|
|
ENST00000648466.1:c.*943A>G
|
ENSP00000497591.1:n.*943A>G
|
|
XM_005272145.2:c.1483A>G
|
XP_005272202.1:p.Ser495Gly
|
|
XM_005272145.3:c.1483A>G
|
XP_005272202.1:p.Ser495Gly
|
|
XM_005272146.3:c.1402A>G
|
XP_005272203.1:p.Ser468Gly
|
|
XM_006714739.2:c.1357A>G
|
XP_006714802.1:p.Ser453Gly
|
|
XM_006714739.3:c.1357A>G
|
XP_006714802.1:p.Ser453Gly
|
|
XM_011543759.1:c.1423A>G
|
XP_011542061.1:p.Ser475Gly
|
|
XM_011543759.3:c.1423A>G
|
XP_011542061.1:p.Ser475Gly
|
|
XM_011543760.1:c.1420A>G
|
XP_011542062.1:p.Ser474Gly
|
|
XM_011543760.2:c.1420A>G
|
XP_011542062.1:p.Ser474Gly
|
|
XM_011543761.1:c.1366A>G
|
XP_011542063.1:p.Ser456Gly
|
|
XM_011543761.2:c.1366A>G
|
XP_011542063.1:p.Ser456Gly
|
|
XM_011543762.1:c.1132A>G
|
XP_011542064.1:p.Ser378Gly
|
|
XM_011543763.1:c.1018A>G
|
XP_011542065.1:p.Ser340Gly
|
|
XM_011543764.1:c.865A>G
|
XP_011542066.1:p.Ser289Gly
|
