ENST00000309383.6:c.2141T>A
MANE Select
|
ENSP00000310649.1:p.Leu714Gln
|
|
ENST00000309383.5:c.2141T>A
|
ENSP00000310649.1:p.Leu714Gln
|
|
ENST00000326848.7:c.1226T>A
|
ENSP00000320853.7:p.Leu409Gln
|
|
ENST00000590333.5:c.2189T>A
|
ENSP00000468190.1:p.Leu730Gln
|
|
NM_032430.1:c.2141T>A
|
NP_115806.1:p.Leu714Gln
|
|
XM_005259327.2:c.1871T>A
|
XP_005259384.1:p.Leu624Gln
|
|
XM_011527395.1:c.1898T>A
|
XP_011525697.1:p.Leu633Gln
|
|
XR_430213.2:n.2124T>A
|
|
|
XM_005259327.3:c.1871T>A
|
XP_005259384.1:p.Leu624Gln
|
|
XM_011527395.2:c.1613T>A
|
XP_011525697.2:p.Leu538Gln
|
|
XM_024451739.1:c.1916T>A
|
XP_024307507.1:p.Leu639Gln
|
|
XR_430213.4:n.2422T>A
|
|
|
NM_032430.2:c.2141T>A
MANE Select
|
NP_115806.1:p.Leu714Gln
|
|