ENST00000703986.1:c.7127A>G
|
ENSP00000515603.1:p.Asp2376Gly
|
|
ENST00000703987.1:c.7127A>G
|
ENSP00000515604.1:p.Asp2376Gly
|
|
ENST00000704649.1:c.3685-3084A>G
|
ENSP00000515974.1:n.3685-3084A>G
|
|
ENST00000704650.1:c.7112A>G
|
ENSP00000515975.1:p.Asp2371Gly
|
|
ENST00000704651.1:c.6959A>G
|
ENSP00000515976.1:p.Asp2320Gly
|
|
ENST00000704652.1:c.6211A>G
|
|
|
ENST00000704654.1:c.3991A>G
|
|
|
ENST00000704655.1:c.3255A>G
|
ENSP00000515980.1:n.3255A>G
|
|
ENST00000704656.1:c.2563A>G
|
ENSP00000515981.1:n.2563A>G
|
|
ENST00000324545.9:c.7112A>G
|
ENSP00000316357.6:p.Asp2371Gly
|
|
ENST00000378308.7:c.7112A>G
MANE Select
|
ENSP00000367558.2:p.Asp2371Gly
|
|
ENST00000324545.8:c.7112A>G
|
ENSP00000316357.6:p.Asp2371Gly
|
|
ENST00000378308.6:c.7112A>G
|
ENSP00000367558.2:p.Asp2371Gly
|
|
ENST00000485180.1:n.321A>G
|
|
|
NM_001039590.2:c.7112A>G
|
NP_001034679.2:p.Asp2371Gly
|
|
NM_001039591.2:c.7112A>G
|
NP_001034680.2:p.Asp2371Gly
|
|
XM_005272675.3:c.7127A>G
|
XP_005272732.1:p.Asp2376Gly
|
|
XM_005272676.3:c.7127A>G
|
XP_005272733.1:p.Asp2376Gly
|
|
XM_005272675.4:c.7127A>G
|
XP_005272732.1:p.Asp2376Gly
|
|
XM_005272676.4:c.7127A>G
|
XP_005272733.1:p.Asp2376Gly
|
|
NM_001039591.3:c.7112A>G
MANE Select
|
NP_001034680.2:p.Asp2371Gly
|
|
NM_001039590.3:c.7112A>G
|
NP_001034679.2:p.Asp2371Gly
|
|