ENST00000225927.7:c.784G>A
MANE Select
|
ENSP00000225927.1:p.Val262Ile
|
|
ENST00000225927.6:c.784G>A
|
ENSP00000225927.1:p.Val262Ile
|
|
ENST00000586516.5:c.386G>A
|
|
|
ENST00000591587.1:c.360-2059G>A
|
ENSP00000467836.1:n.360-2059G>A
|
|
NM_000263.3:c.784G>A
|
NP_000254.2:p.Val262Ile
|
|
XM_006721920.2:c.23-70G>A
|
XP_006721983.1:n.23-70G>A
|
|
XM_011524840.1:c.23-2059G>A
|
XP_011523142.1:n.23-2059G>A
|
|
XM_017024687.1:c.23-70G>A
|
XP_016880176.1:n.23-70G>A
|
|
XM_024450771.1:c.841G>A
|
XP_024306539.1:p.Val281Ile
|
|
XM_024450772.1:c.23-2059G>A
|
XP_024306540.1:n.23-2059G>A
|
|
NM_000263.4:c.784G>A
MANE Select
|
NP_000254.2:p.Val262Ile
|
|