|
ENST00000326735.13:c.1450G>T
MANE Select
|
ENSP00000327214.8:p.Ala484Ser
|
|
|
ENST00000326735.12:c.1450G>T
|
ENSP00000327214.8:p.Ala484Ser
|
|
|
ENST00000341676.9:c.1435G>T
|
ENSP00000341115.5:p.Ala479Ser
|
|
|
ENST00000452699.5:c.1435G>T
|
ENSP00000413307.1:p.Ala479Ser
|
|
|
ENST00000463860.5:n.1058G>T
|
|
|
|
ENST00000502860.1:n.478G>T
|
|
|
|
ENST00000503552.1:c.127G>T
|
ENSP00000421126.1:p.Ala43Ser
|
|
|
ENST00000509392.1:n.538G>T
|
|
|
|
ENST00000617114.4:c.478G>T
|
ENSP00000478781.1:p.Ala160Ser
|
|
|
NM_001141973.2:c.1435G>T
|
NP_001135445.1:p.Ala479Ser
|
|
|
NM_001141974.2:c.1435G>T
|
NP_001135446.1:p.Ala479Ser
|
|
|
NM_022089.3:c.1450G>T
|
NP_071372.1:p.Ala484Ser
|
|
|
XM_005245809.1:c.1450G>T
|
XP_005245866.1:p.Ala484Ser
|
|
|
XM_005245810.1:c.1447G>T
|
XP_005245867.1:p.Ala483Ser
|
|
|
XM_005245811.1:c.1435G>T
|
XP_005245868.1:p.Ala479Ser
|
|
|
XM_005245812.1:c.1423G>T
|
XP_005245869.1:p.Ala475Ser
|
|
|
XM_005245813.1:c.1450G>T
|
XP_005245870.1:p.Ala484Ser
|
|
|
XM_005245815.1:c.1450G>T
|
XP_005245872.1:p.Ala484Ser
|
|
|
XM_006710512.1:c.1432G>T
|
XP_006710575.1:p.Ala478Ser
|
|
|
XM_006710513.1:c.1408G>T
|
XP_006710576.1:p.Ala470Ser
|
|
|
XM_011541128.1:c.1450G>T
|
XP_011539430.1:p.Ala484Ser
|
|
|
XM_011541129.1:c.1450G>T
|
XP_011539431.1:p.Ala484Ser
|
|
|
XM_017000844.1:c.1450G>T
|
XP_016856333.1:p.Ala484Ser
|
|
|
XM_017000845.1:c.1432G>T
|
XP_016856334.1:p.Ala478Ser
|
|
|
XM_017000846.1:c.1408G>T
|
XP_016856335.1:p.Ala470Ser
|
|
|
XM_017000847.1:c.1420G>T
|
XP_016856336.1:p.Ala474Ser
|
|
|
XM_017000848.1:c.1450G>T
|
XP_016856337.1:p.Ala484Ser
|
|
|
XM_017000849.1:c.1435G>T
|
XP_016856338.1:p.Ala479Ser
|
|
|
XM_017000850.1:c.1450G>T
|
XP_016856339.1:p.Ala484Ser
|
|
|
NM_022089.4:c.1450G>T
MANE Select
|
NP_071372.1:p.Ala484Ser
|
|
|
NM_001141973.3:c.1435G>T
|
NP_001135445.1:p.Ala479Ser
|
|
|
NM_001141974.3:c.1435G>T
|
NP_001135446.1:p.Ala479Ser
|
|
