ENST00000683572.1:n.766C>G
|
|
|
ENST00000341947.7:c.4960C>G
MANE Select
|
ENSP00000339915.2:p.Pro1654Ala
|
|
ENST00000341947.6:c.4960C>G
|
ENSP00000339915.2:p.Pro1654Ala
|
|
ENST00000361917.5:c.4639C>G
|
ENSP00000355123.1:p.Pro1547Ala
|
|
ENST00000374708.8:c.4702C>G
|
ENSP00000363840.4:p.Pro1568Ala
|
|
ENST00000477772.1:n.750C>G
|
|
|
NM_080679.2:c.4639C>G
|
NP_542410.2:p.Pro1547Ala
|
|
NM_080680.2:c.4960C>G
|
NP_542411.2:p.Pro1654Ala
|
|
NM_080681.2:c.4702C>G
|
NP_542412.2:p.Pro1568Ala
|
|
XM_011514298.1:c.4114C>G
|
XP_011512600.1:p.Pro1372Ala
|
|
XM_011514299.1:c.4246C>G
|
XP_011512601.1:p.Pro1416Ala
|
|
XM_011514300.1:c.4066C>G
|
XP_011512602.1:p.Pro1356Ala
|
|
XM_011514301.1:c.4003C>G
|
XP_011512603.1:p.Pro1335Ala
|
|
XM_011514302.1:c.3847C>G
|
XP_011512604.1:p.Pro1283Ala
|
|
XM_011514299.2:c.4246C>G
|
XP_011512601.1:p.Pro1416Ala
|
|
XM_011514300.2:c.4066C>G
|
XP_011512602.1:p.Pro1356Ala
|
|
XM_011514302.2:c.3847C>G
|
XP_011512604.1:p.Pro1283Ala
|
|
XM_017010250.1:c.4960C>G
|
XP_016865739.1:p.Pro1654Ala
|
|
XM_017010251.2:c.3778C>G
|
XP_016865740.1:p.Pro1260Ala
|
|
NM_080680.3:c.4960C>G
MANE Select
|
NP_542411.2:p.Pro1654Ala
|
|
NM_080681.3:c.4702C>G
|
NP_542412.2:p.Pro1568Ala
|
|
NM_080679.3:c.4639C>G
|
NP_542410.2:p.Pro1547Ala
|
|