ENST00000309383.6:c.2159C>A
MANE Select
|
ENSP00000310649.1:p.Pro720His
|
|
ENST00000309383.5:c.2159C>A
|
ENSP00000310649.1:p.Pro720His
|
|
ENST00000326848.7:c.1244C>A
|
ENSP00000320853.7:p.Pro415His
|
|
ENST00000590333.5:c.2207C>A
|
ENSP00000468190.1:p.Pro736His
|
|
NM_032430.1:c.2159C>A
|
NP_115806.1:p.Pro720His
|
|
XM_005259327.2:c.1889C>A
|
XP_005259384.1:p.Pro630His
|
|
XM_011527395.1:c.1916C>A
|
XP_011525697.1:p.Pro639His
|
|
XR_430213.2:n.2142C>A
|
|
|
XM_005259327.3:c.1889C>A
|
XP_005259384.1:p.Pro630His
|
|
XM_011527395.2:c.1631C>A
|
XP_011525697.2:p.Pro544His
|
|
XM_024451739.1:c.1934C>A
|
XP_024307507.1:p.Pro645His
|
|
XR_430213.4:n.2440C>A
|
|
|
NM_032430.2:c.2159C>A
MANE Select
|
NP_115806.1:p.Pro720His
|
|