ENST00000341947.7:c.3321T>G
MANE Select
|
ENSP00000339915.2:p.Pro1107=
|
|
ENST00000341947.6:c.3321T>G
|
ENSP00000339915.2:p.Pro1107=
|
|
ENST00000361917.5:c.3000T>G
|
ENSP00000355123.1:p.Pro1000=
|
|
ENST00000374708.8:c.3063T>G
|
ENSP00000363840.4:p.Pro1021=
|
|
ENST00000477772.1:n.273-5343T>G
|
|
|
NM_080679.2:c.3000T>G
|
NP_542410.2:p.Pro1000=
|
|
NM_080680.2:c.3321T>G
|
NP_542411.2:p.Pro1107=
|
|
NM_080681.2:c.3063T>G
|
NP_542412.2:p.Pro1021=
|
|
XM_011514298.1:c.2475T>G
|
XP_011512600.1:p.Pro825=
|
|
XM_011514299.1:c.2607T>G
|
XP_011512601.1:p.Pro869=
|
|
XM_011514300.1:c.2427T>G
|
XP_011512602.1:p.Pro809=
|
|
XM_011514301.1:c.2364T>G
|
XP_011512603.1:p.Pro788=
|
|
XM_011514302.1:c.2208T>G
|
XP_011512604.1:p.Pro736=
|
|
XM_011514299.2:c.2607T>G
|
XP_011512601.1:p.Pro869=
|
|
XM_011514300.2:c.2427T>G
|
XP_011512602.1:p.Pro809=
|
|
XM_011514302.2:c.2208T>G
|
XP_011512604.1:p.Pro736=
|
|
XM_017010250.1:c.3321T>G
|
XP_016865739.1:p.Pro1107=
|
|
XM_017010251.2:c.2139T>G
|
XP_016865740.1:p.Pro713=
|
|
NM_080680.3:c.3321T>G
MANE Select
|
NP_542411.2:p.Pro1107=
|
|
NM_080681.3:c.3063T>G
|
NP_542412.2:p.Pro1021=
|
|
NM_080679.3:c.3000T>G
|
NP_542410.2:p.Pro1000=
|
|