ENST00000683572.1:n.650C>G
|
|
|
ENST00000341947.7:c.4844C>G
MANE Select
|
ENSP00000339915.2:p.Pro1615Arg
|
|
ENST00000341947.6:c.4844C>G
|
ENSP00000339915.2:p.Pro1615Arg
|
|
ENST00000361917.5:c.4523C>G
|
ENSP00000355123.1:p.Pro1508Arg
|
|
ENST00000374708.8:c.4586C>G
|
ENSP00000363840.4:p.Pro1529Arg
|
|
ENST00000477772.1:n.634C>G
|
|
|
NM_080679.2:c.4523C>G
|
NP_542410.2:p.Pro1508Arg
|
|
NM_080680.2:c.4844C>G
|
NP_542411.2:p.Pro1615Arg
|
|
NM_080681.2:c.4586C>G
|
NP_542412.2:p.Pro1529Arg
|
|
XM_011514298.1:c.3998C>G
|
XP_011512600.1:p.Pro1333Arg
|
|
XM_011514299.1:c.4130C>G
|
XP_011512601.1:p.Pro1377Arg
|
|
XM_011514300.1:c.3950C>G
|
XP_011512602.1:p.Pro1317Arg
|
|
XM_011514301.1:c.3887C>G
|
XP_011512603.1:p.Pro1296Arg
|
|
XM_011514302.1:c.3731C>G
|
XP_011512604.1:p.Pro1244Arg
|
|
XM_011514299.2:c.4130C>G
|
XP_011512601.1:p.Pro1377Arg
|
|
XM_011514300.2:c.3950C>G
|
XP_011512602.1:p.Pro1317Arg
|
|
XM_011514302.2:c.3731C>G
|
XP_011512604.1:p.Pro1244Arg
|
|
XM_017010250.1:c.4844C>G
|
XP_016865739.1:p.Pro1615Arg
|
|
XM_017010251.2:c.3662C>G
|
XP_016865740.1:p.Pro1221Arg
|
|
NM_080680.3:c.4844C>G
MANE Select
|
NP_542411.2:p.Pro1615Arg
|
|
NM_080681.3:c.4586C>G
|
NP_542412.2:p.Pro1529Arg
|
|
NM_080679.3:c.4523C>G
|
NP_542410.2:p.Pro1508Arg
|
|