ENST00000244741.10:c.19G>C
MANE Select
|
ENSP00000244741.6:p.Asp7His
|
|
ENST00000244741.9:c.19G>C
|
ENSP00000244741.5:p.Asp7His
|
|
ENST00000373711.3:c.19G>C
|
ENSP00000362815.1:p.Asp7His
|
|
ENST00000405375.5:c.19G>C
|
ENSP00000384849.1:p.Asp7His
|
|
ENST00000448526.6:c.19G>C
|
ENSP00000409259.3:p.Asp7His
|
|
ENST00000459970.1:n.213G>C
|
|
|
ENST00000478800.1:n.238G>C
|
|
|
ENST00000615513.4:c.19G>C
|
ENSP00000482768.1:p.Asp7His
|
|
NM_000389.4:c.19G>C
|
NP_000380.1:p.Asp7His
|
|
NM_001220777.1:c.19G>C
|
NP_001207706.1:p.Asp7His
|
|
NM_001220778.1:c.19G>C
|
NP_001207707.1:p.Asp7His
|
|
NM_001291549.1:c.121G>C
|
NP_001278478.1:p.Asp41His
|
|
NM_078467.2:c.19G>C
|
NP_510867.1:p.Asp7His
|
|
NM_000389.5:c.19G>C
MANE Select
|
NP_000380.1:p.Asp7His
|
|
NM_001220777.2:c.19G>C
|
NP_001207706.1:p.Asp7His
|
|
NM_001220778.2:c.19G>C
|
NP_001207707.1:p.Asp7His
|
|
NM_001291549.3:c.121G>C
|
NP_001278478.1:p.Asp41His
|
|
NM_001374509.1:c.121G>C
|
NP_001361438.1:p.Asp41His
|
|
NM_001374510.1:c.58G>C
|
NP_001361439.1:p.Asp20His
|
|
NM_001374511.1:c.19G>C
|
NP_001361440.1:p.Asp7His
|
|
NM_001374512.1:c.19G>C
|
NP_001361441.1:p.Asp7His
|
|
NM_001374513.1:c.19G>C
|
NP_001361442.1:p.Asp7His
|
|
NM_078467.3:c.19G>C
|
NP_510867.1:p.Asp7His
|
|