ENST00000348729.8:c.917C=
MANE Select
|
ENSP00000302701.4:p.Pro306=
|
|
ENST00000348729.7:c.917C=
|
ENSP00000302701.4:p.Pro306=
|
|
ENST00000353963.7:c.929C=
|
ENSP00000302851.5:p.Pro310=
|
|
ENST00000504513.1:c.164+270C=
|
|
|
ENST00000506512.1:n.528C=
|
|
|
NM_005847.4:c.917C=
|
NP_005838.3:p.Pro306=
|
|
NM_152685.3:c.929C=
|
NP_689898.2:p.Pro310=
|
|
XM_005272148.3:c.1037C=
|
XP_005272205.3:p.Pro346=
|
|
XM_005272149.3:c.1025C=
|
XP_005272206.3:p.Pro342=
|
|
XM_006714741.2:c.1037C=
|
XP_006714804.2:p.Pro346=
|
|
XM_011543765.1:c.1037C=
|
XP_011542067.1:p.Pro346=
|
|
XM_011543766.1:c.818C=
|
XP_011542068.1:p.Pro273=
|
|
XM_011543767.1:c.722C=
|
XP_011542069.1:p.Pro241=
|
|
XM_011543768.1:c.602C=
|
XP_011542070.1:p.Pro201=
|
|
XM_011543769.1:c.212C=
|
XP_011542071.1:p.Pro71=
|
|
XM_005272149.4:c.1025C=
|
XP_005272206.3:p.Pro342=
|
|
XM_011543765.2:c.1037C=
|
XP_011542067.1:p.Pro346=
|
|
NM_005847.5:c.917C=
MANE Select
|
NP_005838.3:p.Pro306=
|
|
NM_152685.4:c.929C=
|
NP_689898.2:p.Pro310=
|
|