ENST00000635120.2:c.303-7453G=
MANE Select
|
ENSP00000489225.1:n.303-7453G=
|
|
ENST00000400186.7:c.303-7453G=
|
ENSP00000383047.3:n.303-7453G=
|
|
ENST00000520002.5:c.303-7453G=
|
ENSP00000430733.1:n.303-7453G=
|
|
ENST00000602557.5:c.303-7453G=
|
ENSP00000473359.1:n.303-7453G=
|
|
ENST00000602723.5:c.303-7453G=
|
ENSP00000473617.1:n.303-7453G=
|
|
ENST00000635120.1:c.303-7453G=
|
ENSP00000489225.1:n.303-7453G=
|
|
NM_033225.5:c.303-7453G=
|
NP_150094.5:n.303-7453G=
|
|
XM_011534752.1:c.303-7453G=
|
XP_011533054.1:n.303-7453G=
|
|
XM_011534752.2:c.303-7453G=
|
XP_011533054.1:n.303-7453G=
|
|
XM_017013731.1:c.303-7453G=
|
XP_016869220.1:n.303-7453G=
|
|
NM_033225.6:c.303-7453G=
MANE Select
|
NP_150094.5:n.303-7453G=
|
|