ENST00000696809.1:c.*1562A>C
|
ENSP00000512887.1:n.*1562A>C
|
|
ENST00000699276.1:c.*616A>C
|
ENSP00000514257.1:n.*616A>C
|
|
ENST00000323584.10:c.2988A>C
MANE Select
|
ENSP00000313504.5:p.Arg996Ser
|
|
ENST00000299167.12:c.2988A>C
|
ENSP00000299167.8:p.Arg996Ser
|
|
ENST00000323584.9:c.2988A>C
|
ENSP00000313504.5:p.Arg996Ser
|
|
ENST00000564711.2:c.2A>C
|
|
|
ENST00000566044.5:c.2967A>C
|
ENSP00000456729.1:p.Arg989Ser
|
|
ENST00000566319.2:n.1804A>C
|
|
|
NM_000293.2:c.2988A>C
|
NP_000284.1:p.Arg996Ser
|
|
NM_001031835.2:c.2967A>C
|
NP_001027005.1:p.Arg989Ser
|
|
XM_005255983.3:c.2988A>C
|
XP_005256040.1:p.Arg996Ser
|
|
XM_005255984.3:c.2967A>C
|
XP_005256041.1:p.Arg989Ser
|
|
XM_011523107.1:c.1566A>C
|
XP_011521409.1:p.Arg522Ser
|
|
NM_001363837.1:c.2988A>C
|
NP_001350766.1:p.Arg996Ser
|
|
XM_005255983.4:c.2988A>C
|
XP_005256040.1:p.Arg996Ser
|
|
XM_005255984.4:c.2967A>C
|
XP_005256041.1:p.Arg989Ser
|
|
XM_017023282.1:c.1875A>C
|
XP_016878771.1:p.Arg625Ser
|
|
XM_017023283.1:c.1566A>C
|
XP_016878772.1:p.Arg522Ser
|
|
XM_017023284.1:c.1566A>C
|
XP_016878773.1:p.Arg522Ser
|
|
XR_001751913.1:n.2912A>C
|
|
|
NM_000293.3:c.2988A>C
MANE Select
|
NP_000284.1:p.Arg996Ser
|
|
NM_001031835.3:c.2967A>C
|
NP_001027005.1:p.Arg989Ser
|
|