ENST00000347401.8:c.169G=
|
|
|
ENST00000353578.9:c.6906G=
|
ENSP00000315873.4:p.Met2302=
|
|
ENST00000295550.9:c.7524G=
MANE Select
|
ENSP00000295550.4:p.Met2508=
|
|
ENST00000295550.8:c.7524G=
|
ENSP00000295550.4:p.Met2508=
|
|
ENST00000347401.7:c.5700G=
|
ENSP00000315609.4:p.Met1900=
|
|
ENST00000353578.8:c.6906G=
|
ENSP00000315873.4:p.Met2302=
|
|
ENST00000409809.5:c.6906G=
|
ENSP00000386844.1:p.Met2302=
|
|
ENST00000472056.5:c.5703G=
|
ENSP00000418285.1:p.Met1901=
|
|
ENST00000491769.1:n.1778G=
|
|
|
NM_004369.3:c.7524G= , LRG_473t1:c.7524G=
|
NP_004360.2:p.Met2508=
|
|
NM_057166.4:c.5703G=
|
NP_476507.3:p.Met1901=
|
|
NM_057167.3:c.6906G=
|
NP_476508.2:p.Met2302=
|
|
XM_005246065.1:c.6924G=
|
XP_005246122.1:p.Met2308=
|
|
XM_005246066.1:c.6303G=
|
XP_005246123.1:p.Met2101=
|
|
XM_006712253.1:c.7023G=
|
XP_006712316.1:p.Met2341=
|
|
XM_011510574.1:c.7521G=
|
XP_011508876.1:p.Met2507=
|
|
XM_011510575.1:c.5118G=
|
XP_011508877.1:p.Met1706=
|
|
XM_017003304.1:c.5118G=
|
XP_016858793.1:p.Met1706=
|
|
XM_024452684.1:c.6303G=
|
XP_024308452.1:p.Met2101=
|
|
NM_004369.4:c.7524G=
MANE Select
|
NP_004360.2:p.Met2508=
|
|
NM_057166.5:c.5703G=
|
NP_476507.3:p.Met1901=
|
|
NM_057167.4:c.6906G=
|
NP_476508.2:p.Met2302=
|
|