ENST00000299084.9:c.64A>G
MANE Select
|
ENSP00000299084.4:p.Met22Val
|
|
ENST00000299084.8:c.64A>G
|
ENSP00000299084.4:p.Met22Val
|
|
ENST00000561205.1:n.402A>G
|
|
|
ENST00000561317.1:c.1A>G
|
ENSP00000453680.1:p.Met1Val
|
|
NM_152594.2:c.64A>G
|
NP_689807.1:p.Met22Val
|
|
XM_005254202.2:c.100A>G
|
XP_005254259.1:p.Met34Val
|
|
XM_005254203.3:c.-15-22837A>G
|
XP_005254260.1:n.-15-22837A>G
|
|
XM_011521288.1:c.1A>G
|
XP_011519590.1:p.Met1Val
|
|
XM_011521289.1:c.1A>G
|
XP_011519591.1:p.Met1Val
|
|
XM_011521290.1:c.1A>G
|
XP_011519592.1:p.Met1Val
|
|
XM_005254202.3:c.100A>G
|
XP_005254259.1:p.Met34Val
|
|
XM_011521289.3:c.1A>G
|
XP_011519591.1:p.Met1Val
|
|
NM_152594.3:c.64A>G
MANE Select
|
NP_689807.1:p.Met22Val
|
|