ENST00000305242.10:c.2734C>T
MANE Select
|
ENSP00000306410.5:p.Gln912Ter
|
|
ENST00000672841.1:c.1810C>T
|
ENSP00000499983.1:p.Gln604Ter
|
|
ENST00000672877.1:c.1309C>T
|
ENSP00000500120.1:p.Gln437Ter
|
|
ENST00000673384.1:c.1810C>T
|
ENSP00000500856.1:p.Gln604Ter
|
|
ENST00000673439.1:c.2734C>T
|
ENSP00000500782.1:p.Gln912Ter
|
|
ENST00000305242.9:c.2734C>T
|
ENSP00000306410.5:p.Gln912Ter
|
|
NM_001290020.1:c.2734C>T
|
NP_001276949.1:p.Gln912Ter
|
|
NM_001290021.1:c.1309C>T
|
NP_001276950.1:p.Gln437Ter
|
|
NM_001312689.1:c.1810C>T
|
NP_001299618.1:p.Gln604Ter
|
|
NM_018076.3:c.2734C>T
|
NP_060546.2:p.Gln912Ter
|
|
NM_018076.4:c.2734C>T
|
NP_060546.2:p.Gln912Ter
|
|
XM_011519526.1:c.2734C>T
|
XP_011517828.1:p.Gln912Ter
|
|
XM_011519527.1:c.2734C>T
|
XP_011517829.1:p.Gln912Ter
|
|
XM_011519528.1:c.2734C>T
|
XP_011517830.1:p.Gln912Ter
|
|
XM_011519529.1:c.2734C>T
|
XP_011517831.1:p.Gln912Ter
|
|
XM_011519530.1:c.2734C>T
|
XP_011517832.1:p.Gln912Ter
|
|
XM_011519531.1:c.2734C>T
|
XP_011517833.1:p.Gln912Ter
|
|
XM_011519532.1:c.2524C>T
|
XP_011517834.1:p.Gln842Ter
|
|
XM_011519533.1:c.1810C>T
|
XP_011517835.1:p.Gln604Ter
|
|
XM_011519534.1:c.1810C>T
|
XP_011517836.1:p.Gln604Ter
|
|
XM_011519535.1:c.1648C>T
|
XP_011517837.1:p.Gln550Ter
|
|
XM_011519537.1:c.1309C>T
|
XP_011517839.1:p.Gln437Ter
|
|
XM_024448049.1:c.2863C>T
|
XP_024303817.1:p.Gln955Ter
|
|
XM_024448050.1:c.2863C>T
|
XP_024303818.1:p.Gln955Ter
|
|
XM_024448051.1:c.2863C>T
|
XP_024303819.1:p.Gln955Ter
|
|
XM_024448052.1:c.2863C>T
|
XP_024303820.1:p.Gln955Ter
|
|
XM_024448053.1:c.2863C>T
|
XP_024303821.1:p.Gln955Ter
|
|
XM_024448054.1:c.2653C>T
|
XP_024303822.1:p.Gln885Ter
|
|
XM_024448055.1:c.1939C>T
|
XP_024303823.1:p.Gln647Ter
|
|
XM_024448056.1:c.1939C>T
|
XP_024303824.1:p.Gln647Ter
|
|
XM_024448057.1:c.1777C>T
|
XP_024303825.1:p.Gln593Ter
|
|
XM_024448058.1:c.1438C>T
|
XP_024303826.1:p.Gln480Ter
|
|
NM_001290020.2:c.2734C>T
|
NP_001276949.1:p.Gln912Ter
|
|
NM_001290021.2:c.1309C>T
|
NP_001276950.1:p.Gln437Ter
|
|
NM_001312689.2:c.1810C>T
|
NP_001299618.1:p.Gln604Ter
|
|
NM_018076.5:c.2734C>T
MANE Select
|
NP_060546.2:p.Gln912Ter
|
|