ENST00000367400.8:c.4042A>G
MANE Select
|
ENSP00000356370.3:p.Ile1348Val
|
|
ENST00000367399.6:c.3706A>G
|
ENSP00000356369.2:p.Ile1236Val
|
|
ENST00000367400.7:c.4042A>G
|
ENSP00000356370.3:p.Ile1348Val
|
|
ENST00000448952.1:c.276A>G
|
ENSP00000395407.1:n.276A>G
|
|
ENST00000484075.5:c.*153A>G
|
ENSP00000433932.1:n.*153A>G
|
|
ENST00000535699.5:c.3970A>G
|
ENSP00000438786.1:p.Ile1324Val
|
|
ENST00000538660.5:c.2434A>G
|
ENSP00000438091.1:p.Ile812Val
|
|
NM_001193640.1:c.3706A>G
|
NP_001180569.1:p.Ile1236Val
|
|
NM_001257965.1:c.3970A>G
|
NP_001244894.1:p.Ile1324Val
|
|
NM_001257966.1:c.2434A>G
|
NP_001244895.1:p.Ile812Val
|
|
NM_201253.2:c.4042A>G
|
NP_957705.1:p.Ile1348Val
|
|
NR_047563.1:n.4043A>G
|
|
|
NR_047564.1:n.4493A>G
|
|
|
XM_011509366.1:c.*147A>G
|
XP_011507668.1:n.*147A>G
|
|
XM_011509367.1:c.*21A>G
|
XP_011507669.1:n.*21A>G
|
|
XM_011509368.1:c.3460A>G
|
XP_011507670.1:p.Ile1154Val
|
|
XM_011509369.1:c.2485A>G
|
XP_011507671.1:p.Ile829Val
|
|
XM_011509369.2:c.2485A>G
|
XP_011507671.1:p.Ile829Val
|
|
XM_017000851.1:c.3199A>G
|
XP_016856340.1:p.Ile1067Val
|
|
XM_017000852.1:c.4177A>G
|
XP_016856341.1:p.Ile1393Val
|
|
NM_201253.3:c.4042A>G
MANE Select
|
NP_957705.1:p.Ile1348Val
|
|
NM_001193640.2:c.3706A>G
|
NP_001180569.1:p.Ile1236Val
|
|
NM_001257965.2:c.3970A>G
|
NP_001244894.1:p.Ile1324Val
|
|
NR_047563.2:n.3995A>G
|
|
|
NR_047564.2:n.4445A>G
|
|
|
NM_001257966.2:c.2434A>G
|
NP_001244895.1:p.Ile812Val
|
|