|
ENST00000458511.7:c.324+13C>G
(TRAPPC2)
|
ENSP00000392495.3:n.324+13C>G
|
|
|
ENST00000518847.2:c.324+13C>G
(TRAPPC2)
|
ENSP00000428900.2:n.324+13C>G
|
|
|
ENST00000683569.1:c.324+13C>G
(TRAPPC2)
|
ENSP00000508155.1:n.324+13C>G
|
|
|
ENST00000683983.1:c.426+13C>G
(TRAPPC2)
|
ENSP00000507474.1:n.426+13C>G
|
|
|
ENST00000380579.6:c.324+13C>G
(TRAPPC2)
MANE Select
|
ENSP00000369953.1:n.324+13C>G
|
|
|
ENST00000359680.9:c.324+13C>G
(TRAPPC2)
|
ENSP00000352708.5:n.324+13C>G
|
|
|
ENST00000380578.1:n.2614C>G
(TRAPPC2)
|
|
|
|
ENST00000380579.5:c.324+13C>G
(TRAPPC2)
|
ENSP00000369953.1:n.324+13C>G
|
|
|
ENST00000458511.6:c.426+13C>G
(TRAPPC2)
|
ENSP00000392495.2:n.426+13C>G
|
|
|
ENST00000517553.1:n.284C>G
(TRAPPC2)
|
|
|
|
ENST00000519382.1:n.957C>G
(TRAPPC2)
|
|
|
|
ENST00000519885.5:c.337C>G
(TRAPPC2)
|
ENSP00000430725.1:p.Leu113Val
|
|
|
NM_001011658.3:c.324+13C>G
(TRAPPC2)
|
NP_001011658.1:n.324+13C>G
|
|
|
NM_001128835.2:c.426+13C>G
(TRAPPC2)
|
NP_001122307.2:n.426+13C>G
|
|
|
NM_014563.5:c.324+13C>G
(TRAPPC2)
|
NP_055378.1:n.324+13C>G
|
|
|
XM_005274599.2:c.33+197G>C
(OFD1)
|
XP_005274656.1:n.33+197G>C
|
|
|
XM_005274602.2:c.33+197G>C
(OFD1)
|
XP_005274659.1:n.33+197G>C
|
|
|
XM_005274603.2:c.33+197G>C
(OFD1)
|
XP_005274660.1:n.33+197G>C
|
|
|
XM_011545565.1:c.324+13C>G
(TRAPPC2)
|
XP_011543867.1:n.324+13C>G
|
|
|
XM_011545566.1:c.324+13C>G
(TRAPPC2)
|
XP_011543868.1:n.324+13C>G
|
|
|
XM_011545591.1:c.33+197G>C
(OFD1)
|
XP_011543893.1:n.33+197G>C
|
|
|
XM_011545593.1:c.33+197G>C
(OFD1)
|
XP_011543895.1:n.33+197G>C
|
|
|
XM_011545596.1:c.33+197G>C
(OFD1)
|
XP_011543898.1:n.33+197G>C
|
|
|
XR_247288.2:n.372+197G>C
(OFD1)
|
|
|
|
XM_011545566.2:c.324+13C>G
(TRAPPC2)
|
XP_011543868.1:n.324+13C>G
|
|
|
NM_001011658.4:c.324+13C>G
(TRAPPC2)
MANE Select
|
NP_001011658.1:n.324+13C>G
|
|
|
NM_001128835.3:c.426+13C>G
(TRAPPC2)
|
NP_001122307.2:n.426+13C>G
|
|
|
NM_014563.6:c.324+13C>G
(TRAPPC2)
|
NP_055378.1:n.324+13C>G
|
|
