ENST00000264690.11:c.1668A>C
MANE Select
|
ENSP00000264690.6:p.Lys556Asn
|
|
ENST00000264690.10:c.1668A>C
|
ENSP00000264690.6:p.Lys556Asn
|
|
ENST00000511406.5:n.1729A>C
|
|
|
ENST00000511608.5:c.1811A>C
|
|
|
ENST00000513864.2:c.1472-713A>C
|
ENSP00000424469.2:n.1472-713A>C
|
|
NM_000892.3:c.1668A>C
|
NP_000883.2:p.Lys556Asn
|
|
XM_011531930.1:c.1701A>C
|
XP_011530232.1:p.Lys567Asn
|
|
XM_011531931.1:c.1701A>C
|
XP_011530233.1:p.Lys567Asn
|
|
XM_011531932.1:c.1587A>C
|
XP_011530234.1:p.Lys529Asn
|
|
XM_011531933.1:c.1587A>C
|
XP_011530235.1:p.Lys529Asn
|
|
XM_011531934.1:c.1062A>C
|
XP_011530236.1:p.Lys354Asn
|
|
NM_000892.4:c.1668A>C
|
NP_000883.2:p.Lys556Asn
|
|
NM_001318394.1:c.1472-713A>C
|
NP_001305323.1:n.1472-713A>C
|
|
NM_001318396.1:c.1062A>C
|
NP_001305325.1:p.Lys354Asn
|
|
XM_011531930.2:c.1701A>C
|
XP_011530232.1:p.Lys567Asn
|
|
XM_017008181.1:c.1701A>C
|
XP_016863670.1:p.Lys567Asn
|
|
XM_017008182.1:c.1619-713A>C
|
XP_016863671.1:n.1619-713A>C
|
|
XM_017008183.1:c.1586-713A>C
|
XP_016863672.1:n.1586-713A>C
|
|
XM_017008184.1:c.1062A>C
|
XP_016863673.1:p.Lys354Asn
|
|
NM_000892.5:c.1668A>C
MANE Select
|
NP_000883.2:p.Lys556Asn
|
|
NM_001318394.2:c.1472-713A>C
|
NP_001305323.1:n.1472-713A>C
|
|
NM_001318396.2:c.1062A>C
|
NP_001305325.1:p.Lys354Asn
|
|