ENST00000260197.12:c.529-1467C=
MANE Select
|
ENSP00000260197.6:n.529-1467C=
|
|
ENST00000260197.11:c.529-1467C=
|
ENSP00000260197.6:n.529-1467C=
|
|
ENST00000532451.1:n.481-1467C=
|
|
|
NM_003105.5:c.529-1467C=
|
NP_003096.1:n.529-1467C=
|
|
XM_011542963.1:c.529-1467C=
|
XP_011541265.1:n.529-1467C=
|
|
XM_011542964.1:c.529-1467C=
|
XP_011541266.1:n.529-1467C=
|
|
XM_011542963.3:c.529-1467C=
|
XP_011541265.1:n.529-1467C=
|
|
XM_017018169.2:c.217-1467C=
|
XP_016873658.1:n.217-1467C=
|
|
XM_017018170.2:c.3+108C=
|
XP_016873659.1:n.3+108C=
|
|
XM_017018171.1:c.529-1467C=
|
XP_016873660.1:n.529-1467C=
|
|
NM_003105.6:c.529-1467C=
MANE Select
|
NP_003096.2:n.529-1467C=
|
|