ENST00000279873.12:c.502+21014G>A
MANE Select
|
ENSP00000279873.7:n.502+21014G>A
|
|
ENST00000644638.1:c.502+21014G>A
|
ENSP00000494412.1:n.502+21014G>A
|
|
ENST00000681100.1:c.502+21014G>A
|
ENSP00000506119.1:n.502+21014G>A
|
|
ENST00000279873.11:c.502+21014G>A
|
ENSP00000279873.7:n.502+21014G>A
|
|
NM_032199.2:c.502+21014G>A
|
NP_115575.1:n.502+21014G>A
|
|
XM_011540262.1:c.502+21014G>A
|
XP_011538564.1:n.502+21014G>A
|
|
XM_024448230.1:c.-66+21014G>A
|
XP_024303998.1:n.-66+21014G>A
|
|
NM_032199.3:c.502+21014G>A
MANE Select
|
NP_115575.1:n.502+21014G>A
|
|