ENST00000290866.10:c.3802G>C
MANE Select
|
ENSP00000290866.4:p.Ala1268Pro
|
|
ENST00000290863.10:c.2080G>C
|
ENSP00000290863.6:p.Ala694Pro
|
|
ENST00000290866.9:c.3802G>C
|
ENSP00000290866.4:p.Ala1268Pro
|
|
ENST00000413513.7:c.1957G>C
|
ENSP00000392247.3:p.Ala653Pro
|
|
ENST00000428043.5:c.*224G>C
|
ENSP00000397593.2:n.*224G>C
|
|
ENST00000577647.2:c.1969+262G>C
|
ENSP00000464149.1:n.1969+262G>C
|
|
ENST00000578839.5:c.*1557G>C
|
ENSP00000462110.2:n.*1557G>C
|
|
ENST00000579314.5:c.*1531G>C
|
ENSP00000462599.1:n.*1531G>C
|
|
NM_000789.3:c.3802G>C
|
NP_000780.1:p.Ala1268Pro
|
|
NM_001178057.1:c.1957G>C
|
NP_001171528.1:p.Ala653Pro
|
|
NM_152830.2:c.2080G>C
|
NP_690043.1:p.Ala694Pro
|
|
XM_005257110.1:c.3253G>C
|
XP_005257167.1:p.Ala1085Pro
|
|
XM_006721737.2:c.2140G>C
|
XP_006721800.2:p.Ala714Pro
|
|
XM_006721737.3:c.2140G>C
|
XP_006721800.2:p.Ala714Pro
|
|
NM_000789.4:c.3802G>C
MANE Select
|
NP_000780.1:p.Ala1268Pro
|
|
NM_001178057.2:c.1957G>C
|
NP_001171528.1:p.Ala653Pro
|
|
NM_152830.3:c.2080G>C
|
NP_690043.1:p.Ala694Pro
|
|
NM_001382700.1:c.3235G>C
|
NP_001369629.1:p.Ala1079Pro
|
|
NM_001382701.1:c.2950G>C
|
NP_001369630.1:p.Ala984Pro
|
|
NM_001382702.1:c.1417G>C
|
NP_001369631.1:p.Ala473Pro
|
|
NR_168483.1:n.2180G>C
|
|
|