ENST00000448821.6:c.1221T>A
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ENSP00000402902.2:p.Pro407=
|
|
ENST00000685871.1:c.1221T>A
|
ENSP00000509964.1:p.Pro407=
|
|
ENST00000686159.1:n.1260T>A
|
|
|
ENST00000686486.1:n.229T>A
|
|
|
ENST00000687302.1:n.1307T>A
|
|
|
ENST00000687357.1:c.1221T>A
|
ENSP00000509549.1:p.Pro407=
|
|
ENST00000687625.1:n.376T>A
|
|
|
ENST00000687787.1:c.1221T>A
|
ENSP00000509440.1:p.Pro407=
|
|
ENST00000688201.1:n.1253T>A
|
|
|
ENST00000688226.1:n.1153T>A
|
|
|
ENST00000688869.1:n.1527T>A
|
|
|
ENST00000689788.1:c.1015T>A
|
ENSP00000508973.1:n.1015T>A
|
|
ENST00000689898.1:c.1221T>A
|
ENSP00000509651.1:p.Pro407=
|
|
ENST00000690070.1:c.1221T>A
|
ENSP00000509654.1:p.Pro407=
|
|
ENST00000690267.1:c.1085T>A
|
ENSP00000510432.1:n.1085T>A
|
|
ENST00000690552.1:n.1082T>A
|
|
|
ENST00000691138.1:n.1082T>A
|
|
|
ENST00000691969.1:c.796T>A
|
ENSP00000510244.1:n.796T>A
|
|
ENST00000692232.1:n.2377T>A
|
|
|
ENST00000692233.1:c.1085T>A
|
ENSP00000509698.1:n.1085T>A
|
|
ENST00000692380.1:n.376T>A
|
|
|
ENST00000692447.1:n.2333T>A
|
|
|
ENST00000693094.1:c.1221T>A
|
ENSP00000510161.1:p.Pro407=
|
|
ENST00000342694.7:c.1221T>A
MANE Select
|
ENSP00000341083.2:p.Pro407=
|
|
ENST00000342694.6:c.1221T>A
|
ENSP00000341083.2:p.Pro407=
|
|
ENST00000464810.5:n.1221T>A
|
|
|
NM_003995.3:c.1221T>A
|
NP_003986.2:p.Pro407=
|
|
XM_005251478.3:c.1221T>A
|
XP_005251535.1:p.Pro407=
|
|
XM_005251479.3:c.234T>A
|
XP_005251536.1:p.Pro78=
|
|
XM_006716778.2:c.1221T>A
|
XP_006716841.1:p.Pro407=
|
|
XM_011517889.1:c.234T>A
|
XP_011516191.1:p.Pro78=
|
|
XM_011517890.1:c.234T>A
|
XP_011516192.1:p.Pro78=
|
|
XM_011517891.1:c.234T>A
|
XP_011516193.1:p.Pro78=
|
|
XM_011517892.1:c.234T>A
|
XP_011516194.1:p.Pro78=
|
|
XM_011517893.1:c.234T>A
|
XP_011516195.1:p.Pro78=
|
|
XM_011517894.1:c.234T>A
|
XP_011516196.1:p.Pro78=
|
|
XM_024447556.1:c.1221T>A
|
XP_024303324.1:p.Pro407=
|
|
XM_024447557.1:c.1221T>A
|
XP_024303325.1:p.Pro407=
|
|
XM_024447558.1:c.234T>A
|
XP_024303326.1:p.Pro78=
|
|
XM_024447560.1:c.-188T>A
|
XP_024303328.1:n.-188T>A
|
|
XM_024447561.1:c.-188T>A
|
XP_024303329.1:n.-188T>A
|
|
NM_003995.4:c.1221T>A
MANE Select
|
NP_003986.2:p.Pro407=
|
|
NM_001378923.1:c.1221T>A
|
NP_001365852.1:p.Pro407=
|
|