ENST00000532043.2:n.250A>T
|
|
|
ENST00000682266.1:c.1783A>T
|
ENSP00000507766.1:p.Asn595Tyr
|
|
ENST00000682341.1:c.2191A>T
|
ENSP00000508251.1:p.Asn731Tyr
|
|
ENST00000683197.1:c.2191A>T
|
ENSP00000507641.1:p.Asn731Tyr
|
|
ENST00000683411.1:c.1783A>T
|
ENSP00000508397.1:p.Asn595Tyr
|
|
ENST00000683437.1:c.1783A>T
|
ENSP00000508408.1:p.Asn595Tyr
|
|
ENST00000683613.1:n.3227A>T
|
|
|
ENST00000684663.1:c.2188A>T
|
ENSP00000508009.1:p.Asn730Tyr
|
|
ENST00000324559.9:c.2233A>T
MANE Select
|
ENSP00000315371.9:p.Asn745Tyr
|
|
ENST00000648804.1:n.2568A>T
|
|
|
ENST00000324559.8:c.2233A>T
|
ENSP00000315371.8:p.Asn745Tyr
|
|
ENST00000532043.1:n.250A>T
|
|
|
NM_001142649.1:c.2230A>T
|
NP_001136121.1:p.Asn744Tyr
|
|
NM_213599.2:c.2233A>T , LRG_868t1:c.2233A>T
|
NP_998764.1:p.Asn745Tyr
|
|
XM_005252820.2:c.2191A>T
|
XP_005252877.2:p.Asn731Tyr
|
|
XM_005252821.2:c.2188A>T
|
XP_005252878.2:p.Asn730Tyr
|
|
XM_005252822.3:c.2155A>T
|
XP_005252879.1:p.Asn719Tyr
|
|
XM_005252823.3:c.2152A>T
|
XP_005252880.1:p.Asn718Tyr
|
|
XM_011519949.1:c.2140A>T
|
XP_011518251.1:p.Asn714Tyr
|
|
XM_005252820.3:c.2191A>T
|
XP_005252877.2:p.Asn731Tyr
|
|
XM_005252821.3:c.2188A>T
|
XP_005252878.2:p.Asn730Tyr
|
|
XM_005252822.4:c.2155A>T
|
XP_005252879.1:p.Asn719Tyr
|
|
XM_011519949.2:c.2140A>T
|
XP_011518251.1:p.Asn714Tyr
|
|
NM_001142649.2:c.2230A>T
|
NP_001136121.1:p.Asn744Tyr
|
|
NM_213599.3:c.2233A>T
MANE Select
|
NP_998764.1:p.Asn745Tyr
|
|