NM_005245.4:c.12774G>A
MANE Select
|
NP_005236.2:p.Pro4258=
|
ENST00000441802.7:c.12774G>A
MANE Select
|
ENSP00000406229.2:p.Pro4258=
|
NM_005245.3:c.12774G>A
|
NP_005236.2:p.Pro4258=
|
ENST00000441802.6:c.12774G>A
|
ENSP00000406229.2:p.Pro4258=
|
ENST00000500085.2:n.466G>A
|
|
ENST00000507105.1:c.302+268G>A
|
|
ENST00000512772.5:c.76G>A
|
|
ENST00000614102.4:c.12780G>A
|
ENSP00000479573.1:p.Pro4260=
|
XM_005262834.2:c.12774G>A
|
XP_005262891.1:p.Pro4258=
|
XM_005262834.3:c.12774G>A
|
XP_005262891.1:p.Pro4258=
|
XM_005262835.1:c.12774G>A
|
XP_005262892.1:p.Pro4258=
|
XM_005262835.2:c.12774G>A
|
XP_005262892.1:p.Pro4258=
|
XM_006714139.2:c.12774G>A
|
XP_006714202.1:p.Pro4258=
|
XM_006714139.3:c.12774G>A
|
XP_006714202.1:p.Pro4258=
|