ENST00000624552.4:c.14934C>G
|
ENSP00000485357.2:p.His4978Gln
|
|
ENST00000683500.2:c.14991C>G
MANE Select
|
ENSP00000508292.2:p.His4997Gln
|
|
ENST00000623487.1:n.3337C>G
|
|
|
ENST00000624552.3:c.14931C>G
|
ENSP00000485357.1:p.His4977Gln
|
|
NM_001291815.1:c.14991C>G
|
NP_001278744.1:p.His4997Gln
|
|
XM_011518465.1:c.14868C>G
|
XP_011516767.1:p.His4956Gln
|
|
XM_011518466.1:c.14859C>G
|
XP_011516768.1:p.His4953Gln
|
|
XM_011518467.1:c.14814C>G
|
XP_011516769.1:p.His4938Gln
|
|
NM_001291815.2:c.14991C>G
MANE Select
|
NP_001278744.1:p.His4997Gln
|
|
XM_011518465.2:c.14868C>G
|
XP_011516767.1:p.His4956Gln
|
|
XM_011518466.2:c.14859C>G
|
XP_011516768.1:p.His4953Gln
|
|
XM_011518467.2:c.14814C>G
|
XP_011516769.1:p.His4938Gln
|
|
XM_017014585.1:c.11772C>G
|
XP_016870074.1:p.His3924Gln
|
|
XM_017014586.1:c.7569C>G
|
XP_016870075.1:p.His2523Gln
|
|
XR_001746957.1:n.92+177G>C
|
|
|
XR_001746958.1:n.92+177G>C
|
|
|