ENST00000371270.6:c.446C>G
MANE Select
|
ENSP00000360317.3:p.Ala149Gly
|
|
ENST00000371270.5:c.446C>G
|
ENSP00000360317.3:p.Ala149Gly
|
|
ENST00000479946.2:n.750C>G
|
|
|
ENST00000490994.6:c.*232C>G
|
ENSP00000433314.1:n.*232C>G
|
|
ENST00000525991.5:c.*21C>G
|
ENSP00000433842.1:n.*21C>G
|
|
ENST00000526814.5:n.701C>G
|
|
|
ENST00000527420.5:c.446C>G
|
ENSP00000433191.1:p.Ala149Gly
|
|
ENST00000527953.5:n.701C>G
|
|
|
ENST00000533320.5:n.680C>G
|
|
|
ENST00000535898.5:c.140C>G
|
ENSP00000445062.1:p.Ala47Gly
|
|
ENST00000539050.5:c.236C>G
|
ENSP00000442343.2:p.Ala79Gly
|
|
ENST00000623108.3:c.236C>G
|
ENSP00000485110.1:p.Ala79Gly
|
|
ENST00000628935.1:c.188C>G
|
ENSP00000487145.1:p.Ala63Gly
|
|
NM_000770.3:c.446C>G
MANE Select
|
NP_000761.3:p.Ala149Gly
|
|
NM_001198853.1:c.236C>G
|
NP_001185782.1:p.Ala79Gly
|
|
NM_001198854.1:c.140C>G
|
NP_001185783.1:p.Ala47Gly
|
|
NM_001198855.1:c.236C>G
|
NP_001185784.1:p.Ala79Gly
|
|
XR_945610.1:n.542C>G
|
|
|