ENST00000392492.8:c.433C>G
MANE Select
|
ENSP00000376282.2:p.His145Asp
|
|
ENST00000250615.7:c.568C>G
|
ENSP00000250615.2:p.His190Asp
|
|
ENST00000392492.7:c.433C>G
|
ENSP00000376282.2:p.His145Asp
|
|
ENST00000587798.1:c.*210C>G
|
ENSP00000468239.1:n.*210C>G
|
|
NM_001088.2:c.433C>G
|
NP_001079.1:p.His145Asp
|
|
NM_001166579.1:c.568C>G
|
NP_001160051.1:p.His190Asp
|
|
NR_110548.1:n.744C>G
|
|
|
XM_011524415.1:c.433C>G
|
XP_011522717.1:p.His145Asp
|
|
XM_011524416.1:c.640C>G
|
XP_011522718.1:p.His214Asp
|
|
XM_011524417.1:c.640C>G
|
XP_011522719.1:p.His214Asp
|
|
XM_011524418.1:c.640C>G
|
XP_011522720.1:p.His214Asp
|
|
XM_011524419.1:c.640C>G
|
XP_011522721.1:p.His214Asp
|
|
XM_011524420.1:c.640C>G
|
XP_011522722.1:p.His214Asp
|
|
XM_011524421.1:c.640C>G
|
XP_011522723.1:p.His214Asp
|
|
XM_011524422.1:c.523C>G
|
XP_011522724.1:p.His175Asp
|
|
XM_011524423.1:c.433C>G
|
XP_011522725.1:p.His145Asp
|
|
XM_017024259.1:c.547C>G
|
XP_016879748.1:p.His183Asp
|
|
NM_001088.3:c.433C>G
MANE Select
|
NP_001079.1:p.His145Asp
|
|
NR_110548.2:n.689C>G
|
|
|
NM_001166579.2:c.568C>G
|
NP_001160051.1:p.His190Asp
|
|