ENST00000695853.1:c.6135G>A
|
ENSP00000512218.1:p.Pro2045=
|
|
ENST00000423902.7:c.6135G>A
MANE Select
|
ENSP00000392028.1:p.Pro2045=
|
|
ENST00000423902.6:c.6135G>A
|
ENSP00000392028.1:p.Pro2045=
|
|
ENST00000524602.5:c.1717-9369G>A
|
ENSP00000437061.1:n.1717-9369G>A
|
|
NM_001316690.1:c.1717-9369G>A
|
NP_001303619.1:n.1717-9369G>A
|
|
NM_017780.3:c.6135G>A
|
NP_060250.2:p.Pro2045=
|
|
XM_011517553.1:c.6225G>A
|
XP_011515855.1:p.Pro2075=
|
|
XM_011517554.1:c.6225G>A
|
XP_011515856.1:p.Pro2075=
|
|
XM_011517555.1:c.6225G>A
|
XP_011515857.1:p.Pro2075=
|
|
XM_011517556.1:c.6225G>A
|
XP_011515858.1:p.Pro2075=
|
|
XM_011517557.1:c.4212G>A
|
XP_011515859.1:p.Pro1404=
|
|
XM_011517558.1:c.3762G>A
|
XP_011515860.1:p.Pro1254=
|
|
XM_011517559.1:c.2970G>A
|
XP_011515861.1:p.Pro990=
|
|
XM_011517553.2:c.6225G>A
|
XP_011515855.1:p.Pro2075=
|
|
XM_011517554.3:c.6225G>A
|
XP_011515856.1:p.Pro2075=
|
|
XM_011517555.2:c.6225G>A
|
XP_011515857.1:p.Pro2075=
|
|
XM_017013612.1:c.6225G>A
|
XP_016869101.1:p.Pro2075=
|
|
XM_017013613.1:c.6135G>A
|
XP_016869102.1:p.Pro2045=
|
|
NM_017780.4:c.6135G>A
MANE Select
|
NP_060250.2:p.Pro2045=
|
|