ENST00000397801.6:c.1426_1427insTCCGAT
MANE Select
|
ENSP00000380903.1:p.Gly476delinsValArgTrp
|
|
ENST00000397801.5:c.1426_1427insTCCGAT
|
ENSP00000380903.1:p.Gly476delinsValArgTrp
|
|
ENST00000538940.5:c.1360_1361insTCCGAT
|
ENSP00000441797.1:p.Gly454delinsValArgTrp
|
|
NM_022370.3:c.1426_1427insTCCGAT
|
NP_071765.2:p.Gly476delinsValArgTrp
|
|
XM_011542953.1:c.2398_2399insTCCGAT
|
XP_011541255.1:p.Gly800delinsValArgTrp
|
|
XM_017018122.1:c.1360_1361insTCCGAT
|
XP_016873611.1:p.Gly454delinsValArgTrp
|
|
NM_022370.4:c.1426_1427insTCCGAT
MANE Select
|
NP_071765.2:p.Gly476delinsValArgTrp
|
|