ENST00000367400.8:c.4006-144T>G
MANE Select
|
ENSP00000356370.3:n.4006-144T>G
|
|
ENST00000367399.6:c.3670-144T>G
|
ENSP00000356369.2:n.3670-144T>G
|
|
ENST00000367400.7:c.4006-144T>G
|
ENSP00000356370.3:n.4006-144T>G
|
|
ENST00000448952.1:c.124-28T>G
|
ENSP00000395407.1:n.124-28T>G
|
|
ENST00000484075.5:c.*117-144T>G
|
ENSP00000433932.1:n.*117-144T>G
|
|
ENST00000535699.5:c.3934-144T>G
|
ENSP00000438786.1:n.3934-144T>G
|
|
ENST00000538660.5:c.2398-144T>G
|
ENSP00000438091.1:n.2398-144T>G
|
|
NM_001193640.1:c.3670-144T>G
|
NP_001180569.1:n.3670-144T>G
|
|
NM_001257965.1:c.3934-144T>G
|
NP_001244894.1:n.3934-144T>G
|
|
NM_001257966.1:c.2398-144T>G
|
NP_001244895.1:n.2398-144T>G
|
|
NM_201253.2:c.4006-144T>G
|
NP_957705.1:n.4006-144T>G
|
|
NR_047563.1:n.4007-144T>G
|
|
|
NR_047564.1:n.4457-144T>G
|
|
|
XM_011509366.1:c.4006-28T>G
|
XP_011507668.1:n.4006-28T>G
|
|
XM_011509367.1:c.3879-144T>G
|
XP_011507669.1:n.3879-144T>G
|
|
XM_011509368.1:c.3424-144T>G
|
XP_011507670.1:n.3424-144T>G
|
|
XM_011509369.1:c.2449-144T>G
|
XP_011507671.1:n.2449-144T>G
|
|
XM_011509369.2:c.2449-144T>G
|
XP_011507671.1:n.2449-144T>G
|
|
XM_017000851.1:c.3163-144T>G
|
XP_016856340.1:n.3163-144T>G
|
|
XM_017000852.1:c.4141-144T>G
|
XP_016856341.1:n.4141-144T>G
|
|
NM_201253.3:c.4006-144T>G
MANE Select
|
NP_957705.1:n.4006-144T>G
|
|
NM_001193640.2:c.3670-144T>G
|
NP_001180569.1:n.3670-144T>G
|
|
NM_001257965.2:c.3934-144T>G
|
NP_001244894.1:n.3934-144T>G
|
|
NR_047563.2:n.3959-144T>G
|
|
|
NR_047564.2:n.4409-144T>G
|
|
|
NM_001257966.2:c.2398-144T>G
|
NP_001244895.1:n.2398-144T>G
|
|