ENST00000624552.4:c.14932C>G
|
ENSP00000485357.2:p.His4978Asp
|
|
ENST00000683500.2:c.14989C>G
MANE Select
|
ENSP00000508292.2:p.His4997Asp
|
|
ENST00000623487.1:n.3335C>G
|
|
|
ENST00000624552.3:c.14929C>G
|
ENSP00000485357.1:p.His4977Asp
|
|
NM_001291815.1:c.14989C>G
|
NP_001278744.1:p.His4997Asp
|
|
XM_011518465.1:c.14866C>G
|
XP_011516767.1:p.His4956Asp
|
|
XM_011518466.1:c.14857C>G
|
XP_011516768.1:p.His4953Asp
|
|
XM_011518467.1:c.14812C>G
|
XP_011516769.1:p.His4938Asp
|
|
NM_001291815.2:c.14989C>G
MANE Select
|
NP_001278744.1:p.His4997Asp
|
|
XM_011518465.2:c.14866C>G
|
XP_011516767.1:p.His4956Asp
|
|
XM_011518466.2:c.14857C>G
|
XP_011516768.1:p.His4953Asp
|
|
XM_011518467.2:c.14812C>G
|
XP_011516769.1:p.His4938Asp
|
|
XM_017014585.1:c.11770C>G
|
XP_016870074.1:p.His3924Asp
|
|
XM_017014586.1:c.7567C>G
|
XP_016870075.1:p.His2523Asp
|
|
XR_001746957.1:n.92+179G>C
|
|
|
XR_001746958.1:n.92+179G>C
|
|
|