ENST00000225964.10:c.3166C>A
MANE Select
|
ENSP00000225964.6:p.Pro1056Thr
|
|
ENST00000225964.9:c.3166C>A
|
ENSP00000225964.5:p.Pro1056Thr
|
|
ENST00000511732.1:n.110C>A
|
|
|
NM_000088.3:c.3166C>A , LRG_1t1:c.3166C>A
|
NP_000079.2:p.Pro1056Thr
|
|
XM_005257058.3:c.2896C>A
|
XP_005257115.2:p.Pro966Thr
|
|
XM_005257059.3:c.2248C>A
|
XP_005257116.2:p.Pro750Thr
|
|
XM_011524341.1:c.2968C>A
|
XP_011522643.1:p.Pro990Thr
|
|
XM_005257058.4:c.2896C>A
|
XP_005257115.2:p.Pro966Thr
|
|
XM_005257059.4:c.2248C>A
|
XP_005257116.2:p.Pro750Thr
|
|
NM_000088.4:c.3166C>A
MANE Select
|
NP_000079.2:p.Pro1056Thr
|
|