ENST00000624552.4:c.14933A>G
|
ENSP00000485357.2:p.His4978Arg
|
|
ENST00000683500.2:c.14990A>G
MANE Select
|
ENSP00000508292.2:p.His4997Arg
|
|
ENST00000623487.1:n.3336A>G
|
|
|
ENST00000624552.3:c.14930A>G
|
ENSP00000485357.1:p.His4977Arg
|
|
NM_001291815.1:c.14990A>G
|
NP_001278744.1:p.His4997Arg
|
|
XM_011518465.1:c.14867A>G
|
XP_011516767.1:p.His4956Arg
|
|
XM_011518466.1:c.14858A>G
|
XP_011516768.1:p.His4953Arg
|
|
XM_011518467.1:c.14813A>G
|
XP_011516769.1:p.His4938Arg
|
|
NM_001291815.2:c.14990A>G
MANE Select
|
NP_001278744.1:p.His4997Arg
|
|
XM_011518465.2:c.14867A>G
|
XP_011516767.1:p.His4956Arg
|
|
XM_011518466.2:c.14858A>G
|
XP_011516768.1:p.His4953Arg
|
|
XM_011518467.2:c.14813A>G
|
XP_011516769.1:p.His4938Arg
|
|
XM_017014585.1:c.11771A>G
|
XP_016870074.1:p.His3924Arg
|
|
XM_017014586.1:c.7568A>G
|
XP_016870075.1:p.His2523Arg
|
|
XR_001746957.1:n.92+178T>C
|
|
|
XR_001746958.1:n.92+178T>C
|
|
|