ENST00000341947.7:c.3320C>G
MANE Select
|
ENSP00000339915.2:p.Pro1107Arg
|
|
ENST00000341947.6:c.3320C>G
|
ENSP00000339915.2:p.Pro1107Arg
|
|
ENST00000361917.5:c.2999C>G
|
ENSP00000355123.1:p.Pro1000Arg
|
|
ENST00000374708.8:c.3062C>G
|
ENSP00000363840.4:p.Pro1021Arg
|
|
ENST00000477772.1:n.273-5344C>G
|
|
|
NM_080679.2:c.2999C>G
|
NP_542410.2:p.Pro1000Arg
|
|
NM_080680.2:c.3320C>G
|
NP_542411.2:p.Pro1107Arg
|
|
NM_080681.2:c.3062C>G
|
NP_542412.2:p.Pro1021Arg
|
|
XM_011514298.1:c.2474C>G
|
XP_011512600.1:p.Pro825Arg
|
|
XM_011514299.1:c.2606C>G
|
XP_011512601.1:p.Pro869Arg
|
|
XM_011514300.1:c.2426C>G
|
XP_011512602.1:p.Pro809Arg
|
|
XM_011514301.1:c.2363C>G
|
XP_011512603.1:p.Pro788Arg
|
|
XM_011514302.1:c.2207C>G
|
XP_011512604.1:p.Pro736Arg
|
|
XM_011514299.2:c.2606C>G
|
XP_011512601.1:p.Pro869Arg
|
|
XM_011514300.2:c.2426C>G
|
XP_011512602.1:p.Pro809Arg
|
|
XM_011514302.2:c.2207C>G
|
XP_011512604.1:p.Pro736Arg
|
|
XM_017010250.1:c.3320C>G
|
XP_016865739.1:p.Pro1107Arg
|
|
XM_017010251.2:c.2138C>G
|
XP_016865740.1:p.Pro713Arg
|
|
NM_080680.3:c.3320C>G
MANE Select
|
NP_542411.2:p.Pro1107Arg
|
|
NM_080681.3:c.3062C>G
|
NP_542412.2:p.Pro1021Arg
|
|
NM_080679.3:c.2999C>G
|
NP_542410.2:p.Pro1000Arg
|
|