ENST00000375262.4:c.703G>T
|
ENSP00000364411.2:p.Ala235Ser
|
|
ENST00000375263.8:c.853G>T
MANE Select
|
ENSP00000364412.3:p.Ala285Ser
|
|
ENST00000463517.2:n.2395G>T
|
|
|
ENST00000464104.6:n.1791G>T
|
|
|
ENST00000467499.6:c.*552G>T
|
ENSP00000498077.1:n.*552G>T
|
|
ENST00000494814.6:n.403G>T
|
|
|
ENST00000643789.1:c.3145G>T
|
|
|
ENST00000648146.1:c.991G>T
|
ENSP00000497238.1:n.991G>T
|
|
ENST00000648332.1:c.530G>T
|
ENSP00000497562.1:n.530G>T
|
|
ENST00000650005.1:c.782G>T
|
ENSP00000498121.1:n.782G>T
|
|
ENST00000375262.3:c.703G>T
|
ENSP00000364411.2:p.Ala235Ser
|
|
ENST00000375263.7:c.853G>T
|
ENSP00000364412.3:p.Ala285Ser
|
|
ENST00000464104.5:n.706G>T
|
|
|
ENST00000467499.5:n.113G>T
|
|
|
ENST00000494814.5:n.412G>T
|
|
|
NM_000197.1:c.853G>T
|
NP_000188.1:p.Ala285Ser
|
|
XM_005251970.3:c.493G>T
|
XP_005252027.1:p.Ala165Ser
|
|
XM_011518618.1:c.853G>T
|
XP_011516920.1:p.Ala285Ser
|
|
XM_011518619.1:c.853G>T
|
XP_011516921.1:p.Ala285Ser
|
|
XM_011518620.1:c.745G>T
|
XP_011516922.1:p.Ala249Ser
|
|
NM_000197.2:c.853G>T
MANE Select
|
NP_000188.1:p.Ala285Ser
|
|
XM_011518618.2:c.853G>T
|
XP_011516920.1:p.Ala285Ser
|
|
XM_011518619.2:c.853G>T
|
XP_011516921.1:p.Ala285Ser
|
|
XM_017014671.1:c.853G>T
|
XP_016870160.1:p.Ala285Ser
|
|
XM_017014672.1:c.853G>T
|
XP_016870161.1:p.Ala285Ser
|
|
XM_017014673.2:c.817G>T
|
XP_016870162.1:p.Ala273Ser
|
|
XM_017014674.1:c.745G>T
|
XP_016870163.1:p.Ala249Ser
|
|
XM_017014675.1:c.691G>T
|
XP_016870164.1:p.Ala231Ser
|
|
XM_017014677.1:c.493G>T
|
XP_016870166.1:p.Ala165Ser
|
|
XM_024447529.1:c.691G>T
|
XP_024303297.1:p.Ala231Ser
|
|
XR_002956778.1:n.3325G>T
|
|
|