ENST00000647358.2:c.1256_1257insC
MANE Select
|
ENSP00000494162.1:p.Gln419HisfsTer?
|
|
ENST00000270279.7:c.1256_1257insC
|
ENSP00000270279.3:p.Gln419HisfsTer?
|
|
ENST00000341505.4:c.1118_1119insC
|
ENSP00000340250.4:p.Gln373HisfsTer?
|
|
NM_001130852.1:c.1118_1119insC
|
NP_001124324.1:p.Gln373HisfsTer?
|
|
NM_012116.3:c.1256_1257insC
|
NP_036248.3:p.Gln419HisfsTer?
|
|
XM_005258696.2:c.1256_1257insC
|
XP_005258753.1:p.Gln419HisfsTer?
|
|
XM_011526688.1:c.1256_1257insC
|
XP_011524990.1:p.Gln419HisfsTer?
|
|
XM_011526689.1:c.1118_1119insC
|
XP_011524991.1:p.Gln373HisfsTer?
|
|
XR_935783.1:n.1203_1204insC
|
|
|
NM_012116.4:c.1256_1257insC
MANE Select
|
NP_036248.3:p.Gln419HisfsTer?
|
|
XM_005258696.3:c.1256_1257insC
|
XP_005258753.1:p.Gln419HisfsTer?
|
|
XM_011526688.2:c.1256_1257insC
|
XP_011524990.1:p.Gln419HisfsTer?
|
|
XM_011526689.2:c.1118_1119insC
|
XP_011524991.1:p.Gln373HisfsTer?
|
|
XR_935783.2:n.1208_1209insC
|
|
|