ENST00000367400.8:c.*110G>A
MANE Select
|
ENSP00000356370.3:n.*110G>A
|
|
ENST00000367400.7:c.*110G>A
|
ENSP00000356370.3:n.*110G>A
|
|
ENST00000448952.1:c.565G>A
|
ENSP00000395407.1:n.565G>A
|
|
ENST00000484075.5:c.*442G>A
|
ENSP00000433932.1:n.*442G>A
|
|
ENST00000535699.5:c.*110G>A
|
ENSP00000438786.1:n.*110G>A
|
|
ENST00000538660.5:c.*110G>A
|
ENSP00000438091.1:n.*110G>A
|
|
NM_001193640.1:c.*110G>A
|
NP_001180569.1:n.*110G>A
|
|
NM_001257965.1:c.*110G>A
|
NP_001244894.1:n.*110G>A
|
|
NM_001257966.1:c.*110G>A
|
NP_001244895.1:n.*110G>A
|
|
NM_201253.2:c.*110G>A
|
NP_957705.1:n.*110G>A
|
|
NR_047563.1:n.4332G>A
|
|
|
NR_047564.1:n.4782G>A
|
|
|
XM_011509366.1:c.*436G>A
|
XP_011507668.1:n.*436G>A
|
|
XM_011509367.1:c.*310G>A
|
XP_011507669.1:n.*310G>A
|
|
XM_011509368.1:c.*110G>A
|
XP_011507670.1:n.*110G>A
|
|
XM_011509369.1:c.*110G>A
|
XP_011507671.1:n.*110G>A
|
|
XM_011509369.2:c.*110G>A
|
XP_011507671.1:n.*110G>A
|
|
XM_017000851.1:c.*110G>A
|
XP_016856340.1:n.*110G>A
|
|
XM_017000852.1:c.*110G>A
|
XP_016856341.1:n.*110G>A
|
|
NM_201253.3:c.*110G>A
MANE Select
|
NP_957705.1:n.*110G>A
|
|
NM_001193640.2:c.*110G>A
|
NP_001180569.1:n.*110G>A
|
|
NM_001257965.2:c.*110G>A
|
NP_001244894.1:n.*110G>A
|
|
NR_047563.2:n.4284G>A
|
|
|
NR_047564.2:n.4734G>A
|
|
|
NM_001257966.2:c.*110G>A
|
NP_001244895.1:n.*110G>A
|
|