ENST00000224721.12:c.3639C>A
(CDH23)
MANE Select
|
ENSP00000224721.9:p.Tyr1213Ter
|
|
ENST00000398809.9:c.3636C>A
(CDH23)
|
ENSP00000381789.5:p.Tyr1212Ter
|
|
ENST00000224721.10:c.3654C>A
(CDH23)
|
ENSP00000224721.8:p.Tyr1218Ter
|
|
ENST00000398786.2:c.-6+7200G>T
(C10orf105)
|
ENSP00000381766.3:n.-6+7200G>T
|
|
ENST00000398792.3:n.331C>A
(CDH23)
|
|
|
ENST00000398809.8:c.3636C>A
(CDH23)
|
ENSP00000381789.5:p.Tyr1212Ter
|
|
ENST00000616684.4:c.3639C>A
(CDH23)
|
ENSP00000482036.2:p.Tyr1213Ter
|
|
ENST00000622827.4:c.3639C>A
(CDH23)
|
ENSP00000483211.1:p.Tyr1213Ter
|
|
NM_001168390.1:c.-6+7200G>T
(C10orf105)
|
NP_001161862.1:n.-6+7200G>T
|
|
NM_001171930.1:c.3639C>A
(CDH23)
|
NP_001165401.1:p.Tyr1213Ter
|
|
NM_022124.5:c.3639C>A
(CDH23)
|
NP_071407.4:p.Tyr1213Ter
|
|
XM_006717940.2:c.3834C>A
(CDH23)
|
XP_006718003.1:p.Tyr1278Ter
|
|
XM_006717942.2:c.3768C>A
(CDH23)
|
XP_006718005.1:p.Tyr1256Ter
|
|
XM_011540039.1:c.3834C>A
(CDH23)
|
XP_011538341.1:p.Tyr1278Ter
|
|
XM_011540040.1:c.3828C>A
(CDH23)
|
XP_011538342.1:p.Tyr1276Ter
|
|
XM_011540041.1:c.3774C>A
(CDH23)
|
XP_011538343.1:p.Tyr1258Ter
|
|
XM_011540042.1:c.3834C>A
(CDH23)
|
XP_011538344.1:p.Tyr1278Ter
|
|
XM_011540043.1:c.3834C>A
(CDH23)
|
XP_011538345.1:p.Tyr1278Ter
|
|
XM_011540044.1:c.3699C>A
(CDH23)
|
XP_011538346.1:p.Tyr1233Ter
|
|
XM_011540045.1:c.3834C>A
(CDH23)
|
XP_011538347.1:p.Tyr1278Ter
|
|
XM_011540046.1:c.3294C>A
(CDH23)
|
XP_011538348.1:p.Tyr1098Ter
|
|
XM_011540047.1:c.2652C>A
(CDH23)
|
XP_011538349.1:p.Tyr884Ter
|
|
XM_011540048.1:c.3834C>A
(CDH23)
|
XP_011538350.1:p.Tyr1278Ter
|
|
XM_011540049.1:c.3834C>A
(CDH23)
|
XP_011538351.1:p.Tyr1278Ter
|
|
XM_011540050.1:c.3834C>A
(CDH23)
|
XP_011538352.1:p.Tyr1278Ter
|
|
XM_011540051.1:c.3834C>A
(CDH23)
|
XP_011538353.1:p.Tyr1278Ter
|
|
XM_011540052.1:c.162C>A
(CDH23)
|
XP_011538354.1:p.Tyr54Ter
|
|
XM_011540053.1:c.3834C>A
(CDH23)
|
XP_011538355.1:p.Tyr1278Ter
|
|
XR_945796.1:n.4077C>A
(CDH23)
|
|
|
NM_001168390.2:c.-6+7200G>T
(C10orf105)
|
NP_001161862.1:n.-6+7200G>T
|
|
NM_001171930.2:c.3639C>A
(CDH23)
|
NP_001165401.1:p.Tyr1213Ter
|
|
NM_022124.6:c.3639C>A
(CDH23)
MANE Select
|
NP_071407.4:p.Tyr1213Ter
|
|