ENST00000254108.12:c.592G>C
MANE Select
|
ENSP00000254108.8:p.Asp198His
|
|
ENST00000254108.11:c.592G>C
|
ENSP00000254108.7:p.Asp198His
|
|
ENST00000380244.7:c.589G>C
|
ENSP00000369594.3:p.Asp197His
|
|
ENST00000487509.6:n.657G>C
|
|
|
ENST00000566605.5:c.592G>C
|
ENSP00000455073.1:p.Asp198His
|
|
ENST00000568685.1:c.592G>C
|
ENSP00000455282.1:p.Asp198His
|
|
NM_001170634.1:c.589G>C
|
NP_001164105.1:p.Asp197His
|
|
NM_001170937.1:c.580G>C
|
NP_001164408.1:p.Asp194His
|
|
NM_004960.3:c.592G>C , LRG_655t1:c.592G>C
|
NP_004951.1:p.Asp198His
|
|
NR_028388.2:n.697G>C
|
|
|
XM_005255233.3:c.12G>C
|
XP_005255290.1:p.Lys4Asn
|
|
XM_011545781.1:c.586G>C
|
XP_011544083.1:p.Asp196His
|
|
XM_011545782.1:c.12G>C
|
XP_011544084.1:p.Lys4Asn
|
|
XM_005255233.5:c.12G>C
|
XP_005255290.1:p.Lys4Asn
|
|
XM_011545782.2:c.12G>C
|
XP_011544084.1:p.Lys4Asn
|
|
XM_024450221.1:c.583G>C
|
XP_024305989.1:p.Asp195His
|
|
NM_004960.4:c.592G>C
MANE Select
|
NP_004951.1:p.Asp198His
|
|