ENST00000332142.10:c.2963-1034T>G
MANE Select
|
ENSP00000331727.5:n.2963-1034T>G
|
|
ENST00000332142.9:c.2963-1034T>G
|
ENSP00000331727.5:n.2963-1034T>G
|
|
ENST00000618399.4:c.2663-1034T>G
|
ENSP00000482818.1:n.2663-1034T>G
|
|
NM_033272.3:c.2963-1034T>G
|
NP_150375.2:n.2963-1034T>G
|
|
XM_011512109.1:c.2987-1034T>G
|
XP_011510411.1:n.2987-1034T>G
|
|
XM_011512109.3:c.2987-1034T>G
|
XP_011510411.1:n.2987-1034T>G
|
|
XM_017005218.2:c.2978-1034T>G
|
XP_016860707.1:n.2978-1034T>G
|
|
XM_017005219.2:c.2954-1034T>G
|
XP_016860708.1:n.2954-1034T>G
|
|
XM_017005220.2:c.2942-1034T>G
|
XP_016860709.1:n.2942-1034T>G
|
|
NM_033272.4:c.2963-1034T>G
MANE Select
|
NP_150375.2:n.2963-1034T>G
|
|