ENST00000347401.8:c.1290C>G
|
|
|
ENST00000353578.9:c.8027C>G
|
ENSP00000315873.4:p.Pro2676Arg
|
|
ENST00000682957.1:c.772C>G
|
|
|
ENST00000684508.1:n.912C>G
|
|
|
ENST00000295550.9:c.8645C>G
MANE Select
|
ENSP00000295550.4:p.Pro2882Arg
|
|
ENST00000295550.8:c.8645C>G
|
ENSP00000295550.4:p.Pro2882Arg
|
|
ENST00000347401.7:c.6821C>G
|
ENSP00000315609.4:p.Pro2274Arg
|
|
ENST00000353578.8:c.8027C>G
|
ENSP00000315873.4:p.Pro2676Arg
|
|
ENST00000409809.5:c.8027C>G
|
ENSP00000386844.1:p.Pro2676Arg
|
|
ENST00000472056.5:c.6824C>G
|
ENSP00000418285.1:p.Pro2275Arg
|
|
ENST00000491769.1:n.5087C>G
|
|
|
NM_004369.3:c.8645C>G , LRG_473t1:c.8645C>G
|
NP_004360.2:p.Pro2882Arg
|
|
NM_057166.4:c.6824C>G
|
NP_476507.3:p.Pro2275Arg
|
|
NM_057167.3:c.8027C>G
|
NP_476508.2:p.Pro2676Arg
|
|
XM_005246065.1:c.8045C>G
|
XP_005246122.1:p.Pro2682Arg
|
|
XM_005246066.1:c.7424C>G
|
XP_005246123.1:p.Pro2475Arg
|
|
XM_006712253.1:c.8144C>G
|
XP_006712316.1:p.Pro2715Arg
|
|
XM_011510574.1:c.8642C>G
|
XP_011508876.1:p.Pro2881Arg
|
|
XM_011510575.1:c.6239C>G
|
XP_011508877.1:p.Pro2080Arg
|
|
XM_017003304.1:c.6239C>G
|
XP_016858793.1:p.Pro2080Arg
|
|
XM_024452684.1:c.7424C>G
|
XP_024308452.1:p.Pro2475Arg
|
|
NM_004369.4:c.8645C>G
MANE Select
|
NP_004360.2:p.Pro2882Arg
|
|
NM_057166.5:c.6824C>G
|
NP_476507.3:p.Pro2275Arg
|
|
NM_057167.4:c.8027C>G
|
NP_476508.2:p.Pro2676Arg
|
|