ENST00000449082.3:c.3229-375T>G
MANE Select
|
ENSP00000390600.2:n.3229-375T>G
|
|
ENST00000643924.1:c.3226-375T>G
|
ENSP00000495595.1:n.3226-375T>G
|
|
ENST00000655275.1:c.3253-375T>G
|
ENSP00000499510.1:n.3253-375T>G
|
|
ENST00000449082.2:c.3229-375T>G
|
ENSP00000390600.2:n.3229-375T>G
|
|
NM_001293306.2:c.3226-375T>G
|
NP_001280235.2:n.3226-375T>G
|
|
NM_001293307.2:c.2935-375T>G
|
NP_001280236.2:n.2935-375T>G
|
|
NM_006514.3:c.3229-375T>G
|
NP_006505.3:n.3229-375T>G
|
|
XM_005265371.2:c.3238-375T>G
|
XP_005265428.1:n.3238-375T>G
|
|
XM_011533993.1:c.3235-375T>G
|
XP_011532295.1:n.3235-375T>G
|
|
XM_011533994.1:c.2944-375T>G
|
XP_011532296.1:n.2944-375T>G
|
|
XM_005265371.3:c.3238-375T>G
|
XP_005265428.1:n.3238-375T>G
|
|
XM_011533993.2:c.3235-375T>G
|
XP_011532295.1:n.3235-375T>G
|
|
XM_011533994.2:c.2944-375T>G
|
XP_011532296.1:n.2944-375T>G
|
|
NM_006514.4:c.3229-375T>G
MANE Select
|
NP_006505.4:n.3229-375T>G
|
|