ENST00000307068.5:c.206-638A>G
(SOSTDC1)
MANE Select
|
ENSP00000304930.4:n.206-638A>G
|
|
ENST00000674759.1:c.-47+32779A>G
(CRPPA)
|
ENSP00000502749.1:n.-47+32779A>G
|
|
ENST00000675257.1:c.-47+32779A>G
(CRPPA)
|
ENSP00000501664.1:n.-47+32779A>G
|
|
ENST00000307068.4:c.206-638A>G
(SOSTDC1)
|
ENSP00000304930.4:n.206-638A>G
|
|
ENST00000396652.1:c.278-638A>G
(SOSTDC1)
|
ENSP00000379889.1:n.278-638A>G
|
|
NM_015464.2:c.206-638A>G
(SOSTDC1)
|
NP_056279.1:n.206-638A>G
|
|
XM_011515502.1:c.-47+32779A>G
(CRPPA)
|
XP_011513804.1:n.-47+32779A>G
|
|
XM_011515503.1:c.-47+32779A>G
(CRPPA)
|
XP_011513805.1:n.-47+32779A>G
|
|
XM_011515504.1:c.-47+32779A>G
(CRPPA)
|
XP_011513806.1:n.-47+32779A>G
|
|
XM_011515505.1:c.-47+32779A>G
(CRPPA)
|
XP_011513807.1:n.-47+32779A>G
|
|
XM_011515506.1:c.-47+32779A>G
(CRPPA)
|
XP_011513808.1:n.-47+32779A>G
|
|
XM_011515507.1:c.-47+32779A>G
(CRPPA)
|
XP_011513809.1:n.-47+32779A>G
|
|
XR_927059.1:n.1117+2285T>C
|
|
|
XM_024446909.1:c.-47+32779A>G
(CRPPA)
|
XP_024302677.1:n.-47+32779A>G
|
|
XM_024446910.1:c.-47+32779A>G
(CRPPA)
|
XP_024302678.1:n.-47+32779A>G
|
|
XM_024446911.1:c.-47+32779A>G
(CRPPA)
|
XP_024302679.1:n.-47+32779A>G
|
|
XR_001745102.1:n.630T>C
|
|
|
NM_015464.3:c.206-638A>G
(SOSTDC1)
MANE Select
|
NP_056279.1:n.206-638A>G
|
|