ENST00000318471.5:c.824C>A
MANE Select
|
ENSP00000315680.3:p.Pro275His
|
|
ENST00000541292.6:c.*89C>A
|
ENSP00000441004.1:n.*89C>A
|
|
ENST00000678002.1:c.512C>A
|
|
|
ENST00000678557.1:c.710C>A
|
ENSP00000502962.1:p.Pro237His
|
|
ENST00000679286.1:c.704C>A
|
ENSP00000503168.1:p.Pro235His
|
|
ENST00000318471.4:c.824C>A
|
ENSP00000315680.3:p.Pro275His
|
|
NM_000288.3:c.824C>A
|
NP_000279.1:p.Pro275His
|
|
XM_005267019.3:c.710C>A
|
XP_005267076.1:p.Pro237His
|
|
XM_006715502.1:c.530C>A
|
XP_006715565.1:p.Pro177His
|
|
XM_011535900.1:c.547C>A
|
XP_011534202.1:p.Leu183Met
|
|
XM_005267019.4:c.710C>A
|
XP_005267076.1:p.Pro237His
|
|
XM_006715502.2:c.530C>A
|
XP_006715565.1:p.Pro177His
|
|
XM_017010934.2:c.547C>A
|
XP_016866423.1:p.Leu183Met
|
|
NM_000288.4:c.824C>A
MANE Select
|
NP_000279.1:p.Pro275His
|
|